Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs619203
rs619203
Entrez Id: 6098
Gene Symbol: ROS1
ROS1
CUI: C0007785
Disease:
Cerebral Infarction
0.010 GeneticVariation BEFREE An initial chi(2) test (false discovery rate <0.05) and subsequent multivariable logistic-regression analysis with adjustment for conventional risk factors (P<0.05) revealed that the -14C-->T polymorphism (rs1800977) of ABCA1, the A-->C (rs3027898) and C-->T (Ser532Leu, rs1059703) polymorphisms of IRAK1, and the G-->C (Cys2229Ser) polymorphism (rs619203) of ROS1 were significantly associated with atherothrombotic cerebral infarction; that the -428G-->A polymorphism (rs710968) of LIMK1 was significantly associated with intracerebral hemorrhage; and that the 13989A-->G (Ile118Val) polymorphism (NC_000007.12) of CYP3A4 was significantly associated with subarachnoid hemorrhage. 18566305 2008
dbSNP: rs619203
rs619203
Entrez Id: 6098
Gene Symbol: ROS1
ROS1
CUI: C0038525
Disease:
Subarachnoid Hemorrhage
0.010 GeneticVariation BEFREE An initial chi(2) test (false discovery rate <0.05) and subsequent multivariable logistic-regression analysis with adjustment for conventional risk factors (P<0.05) revealed that the -14C-->T polymorphism (rs1800977) of ABCA1, the A-->C (rs3027898) and C-->T (Ser532Leu, rs1059703) polymorphisms of IRAK1, and the G-->C (Cys2229Ser) polymorphism (rs619203) of ROS1 were significantly associated with atherothrombotic cerebral infarction; that the -428G-->A polymorphism (rs710968) of LIMK1 was significantly associated with intracerebral hemorrhage; and that the 13989A-->G (Ile118Val) polymorphism (NC_000007.12) of CYP3A4 was significantly associated with subarachnoid hemorrhage. 18566305 2008
dbSNP: rs619203
rs619203
Entrez Id: 6098
Gene Symbol: ROS1
ROS1
CUI: C0011849
Disease:
Diabetes Mellitus
0.010 GeneticVariation BEFREE Evaluation of genotype distributions by the Chi-square test and subsequent multivariable logistic regression analysis with adjustment for age, sex, body mass index, smoking status, and the prevalence of diabetes mellitus and hypercholesterolemia revealed that the -14C-->T polymorphism of ABCA1, the C-->G (Ser2229Cys) polymorphism of ROS1, the C-->T (Asn591Asn) polymorphism of LDLR, the 13989A-->G (Ile118Val) polymorphism of CYP3A4, the C-->G and A-->C polymorphisms of ADIPOR1, and the -519A-->G polymorphism of MMP1 were significantly (P<0.05) associated with the prevalence of hypertension. 18097620 2008
dbSNP: rs619203
rs619203
Entrez Id: 6098
Gene Symbol: ROS1
ROS1
CUI: C0020538
Disease:
Hypertensive disease
0.010 GeneticVariation BEFREE Evaluation of genotype distributions by the Chi-square test and subsequent multivariable logistic regression analysis with adjustment for age, sex, body mass index, smoking status, and the prevalence of diabetes mellitus and hypercholesterolemia revealed that the -14C-->T polymorphism of ABCA1, the C-->G (Ser2229Cys) polymorphism of ROS1, the C-->T (Asn591Asn) polymorphism of LDLR, the 13989A-->G (Ile118Val) polymorphism of CYP3A4, the C-->G and A-->C polymorphisms of ADIPOR1, and the -519A-->G polymorphism of MMP1 were significantly (P<0.05) associated with the prevalence of hypertension. 18097620 2008
dbSNP: rs619203
rs619203
Entrez Id: 6098
Gene Symbol: ROS1
ROS1
CUI: C0020443
Disease:
Hypercholesterolemia
0.010 GeneticVariation BEFREE Evaluation of genotype distributions by the Chi-square test and subsequent multivariable logistic regression analysis with adjustment for age, sex, body mass index, smoking status, and the prevalence of diabetes mellitus and hypercholesterolemia revealed that the -14C-->T polymorphism of ABCA1, the C-->G (Ser2229Cys) polymorphism of ROS1, the C-->T (Asn591Asn) polymorphism of LDLR, the 13989A-->G (Ile118Val) polymorphism of CYP3A4, the C-->G and A-->C polymorphisms of ADIPOR1, and the -519A-->G polymorphism of MMP1 were significantly (P<0.05) associated with the prevalence of hypertension. 18097620 2008
dbSNP: rs750272074
rs750272074
Entrez Id: 6098
Gene Symbol: ROS1
ROS1
CUI: C0007785
Disease:
Cerebral Infarction
0.010 GeneticVariation BEFREE The Chi-square test, multivariable logistic regression analysis with adjustment for age, sex, body mass index, and the prevalence of hypertension, hypercholesterolemia, and diabetes mellitus, as well as a stepwise forward selection procedure revealed that the 2445G-->A (Ala54Thr) polymorphism (rs1799883) of FABP2, the -108/3G-->4G polymorphism of IPF1 (S82168), the A-->G (Thr94Ala) polymorphism (rs2241883) of FABP1, the G-->A (Asp2213Asn) polymorphism (rs529038) of ROS1, the -11377C-->G polymorphism (rs266729) of ADIPOQ, the 162A-->C polymorphism (rs4769055) of ALOX5AP, the -786T-->C polymorphism (rs2070744) of NOS3, and the 3279C-->T polymorphism (rs7291467) of LGALS2 were associated (P<0.05) with the prevalence of atherothrombotic cerebral infarction. 18506375 2008
dbSNP: rs750272074
rs750272074
Entrez Id: 6098
Gene Symbol: ROS1
ROS1
CUI: C0020538
Disease:
Hypertensive disease
0.010 GeneticVariation BEFREE The Chi-square test, multivariable logistic regression analysis with adjustment for age, sex, body mass index, and the prevalence of hypertension, hypercholesterolemia, and diabetes mellitus, as well as a stepwise forward selection procedure revealed that the 2445G-->A (Ala54Thr) polymorphism (rs1799883) of FABP2, the -108/3G-->4G polymorphism of IPF1 (S82168), the A-->G (Thr94Ala) polymorphism (rs2241883) of FABP1, the G-->A (Asp2213Asn) polymorphism (rs529038) of ROS1, the -11377C-->G polymorphism (rs266729) of ADIPOQ, the 162A-->C polymorphism (rs4769055) of ALOX5AP, the -786T-->C polymorphism (rs2070744) of NOS3, and the 3279C-->T polymorphism (rs7291467) of LGALS2 were associated (P<0.05) with the prevalence of atherothrombotic cerebral infarction. 18506375 2008
dbSNP: rs1057519788
rs1057519788
Entrez Id: 6098
Gene Symbol: ROS1
ROS1
CUI: C0152013
Disease:
Adenocarcinoma of lung (disorder)
T 0.700 CausalMutation CLINVAR
dbSNP: rs1057519788
rs1057519788
Entrez Id: 6098
Gene Symbol: ROS1
ROS1
CUI: C0152013
Disease:
Adenocarcinoma of lung (disorder)
T 0.700 GeneticVariation CLINVAR Acquired resistance to crizotinib from a mutation in CD74-ROS1. 23724914 2013
dbSNP: rs61743088
rs61743088
Entrez Id: 6098
Gene Symbol: ROS1
ROS1
CUI: C4021085
Disease:
Abnormality of brain morphology
G 0.700 GeneticVariation CLINVAR
dbSNP: rs776274768
rs776274768
Entrez Id: 6098
Gene Symbol: ROS1
ROS1
CUI: C0349588
Disease:
Short stature
A 0.700 CausalMutation CLINVAR
dbSNP: rs17632578
rs17632578
Entrez Id: 6098
Gene Symbol: ROS1
ROS1
CUI: C0023467
Disease:
Leukemia, Myelocytic, Acute
C 0.700 GeneticVariation GWASCAT Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia. 27903959 2017
dbSNP: rs1894674
rs1894674
Entrez Id: 6098
Gene Symbol: ROS1
ROS1
CUI: C0023467
Disease:
Leukemia, Myelocytic, Acute
C 0.700 GeneticVariation GWASCAT Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia. 27903959 2017
dbSNP: rs210966
rs210966
Entrez Id: 6098
Gene Symbol: ROS1
ROS1
CUI: C0201973
Disease:
Creatine kinase measurement
0.700 GeneticVariation GWASCAT Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases. 29403010 2018
dbSNP: rs210967
rs210967
Entrez Id: 6098
Gene Symbol: ROS1
ROS1
CUI: C0025295
Disease:
Meningitis, Pneumococcal
0.700 GeneticVariation GWASCAT Joint sequencing of human and pathogen genomes reveals the genetics of pneumococcal meningitis. 31092817 2019
dbSNP: rs2157535
rs2157535
Entrez Id: 6098
Gene Symbol: ROS1
ROS1
CUI: C0023467
Disease:
Leukemia, Myelocytic, Acute
G 0.700 GeneticVariation GWASCAT Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia. 27903959 2017
dbSNP: rs2301485
rs2301485
Entrez Id: 6098
Gene Symbol: ROS1
ROS1
CUI: C0023467
Disease:
Leukemia, Myelocytic, Acute
A 0.700 GeneticVariation GWASCAT Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia. 27903959 2017
dbSNP: rs3798379
rs3798379
Entrez Id: 6098
Gene Symbol: ROS1
ROS1
CUI: C0023467
Disease:
Leukemia, Myelocytic, Acute
T 0.700 GeneticVariation GWASCAT Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia. 27903959 2017
dbSNP: rs6913494
rs6913494
Entrez Id: 6098
Gene Symbol: ROS1
ROS1
CUI: C0410702
Disease:
Adolescent idiopathic scoliosis
0.700 GeneticVariation GWASCAT The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease. 30019117 2018
dbSNP: rs6913494
rs6913494
Entrez Id: 6098
Gene Symbol: ROS1
ROS1
CUI: C1837461
Disease:
SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3
0.700 GeneticVariation GWASCAT The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease. 30019117 2018
dbSNP: rs1444274116
rs1444274116
Entrez Id: 6098
Gene Symbol: ROS1
ROS1
CUI: C0278701
Disease:
Gastric Adenocarcinoma
0.700 GeneticVariation UNIPROT