Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs845084
rs845084
Entrez Id: 105378531
Gene Symbol: LINC02641
LINC02641
CUI: C1305855
Disease:
Body mass index
0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs845084
rs845084
Entrez Id: 105378531
Gene Symbol: LINC02641
LINC02641
CUI: C1305855
Disease:
Body mass index
A 0.700 GeneticVariation GWASCAT Meta-analysis of genome-wide association studies for body fat distribution in 694 649 individuals of European ancestry. 30239722 2019
dbSNP: rs11248566
rs11248566
Entrez Id: 105378531
Gene Symbol: LINC02641
LINC02641
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: rs11597044
rs11597044
Entrez Id: 105378531
Gene Symbol: LINC02641
LINC02641
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: rs11597044
rs11597044
Entrez Id: 105378531
Gene Symbol: LINC02641
LINC02641
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: rs1219960
rs1219960
Entrez Id: 105378531
Gene Symbol: LINC02641
LINC02641
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: rs1568079
rs1568079
Entrez Id: 105378531
Gene Symbol: LINC02641
LINC02641
CUI: C1305855
Disease:
Body mass index
A 0.700 GeneticVariation GWASCAT Genome-wide association study identifies 112 new loci for body mass index in the Japanese population. 28892062 2017
dbSNP: rs2282015
rs2282015
Entrez Id: 105378531
Gene Symbol: LINC02641
LINC02641
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: rs4980297
rs4980297
Entrez Id: 105378531
Gene Symbol: LINC02641
LINC02641
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: rs6599698
rs6599698
Entrez Id: 105378531
Gene Symbol: LINC02641
LINC02641
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: rs7090367
rs7090367
Entrez Id: 105378531
Gene Symbol: LINC02641
LINC02641
CUI: C1305855
Disease:
Body mass index
C 0.700 GeneticVariation GWASCAT Genome-wide association study identifies 112 new loci for body mass index in the Japanese population. 28892062 2017
dbSNP: rs7091877
rs7091877
Entrez Id: 105378531
Gene Symbol: LINC02641
LINC02641
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: rs845083
rs845083
Entrez Id: 105378531
Gene Symbol: LINC02641
LINC02641
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: rs845084
rs845084
Entrez Id: 105378531
Gene Symbol: LINC02641
LINC02641
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: rs705145
rs705145
Entrez Id: 105378531
Gene Symbol: LINC02641
LINC02641
CUI: C0026603
Disease:
Motion Sickness
C 0.700 GeneticVariation GWASCAT Genetic variants associated with motion sickness point to roles for inner ear development, neurological processes and glucose homeostasis. 25628336 2015
dbSNP: rs2282015
rs2282015
Entrez Id: 105378531
Gene Symbol: LINC02641
LINC02641
CUI: C1861172
Disease:
Venous Thromboembolism
G 0.700 GeneticVariation GWASDB A genome-wide search for common SNP x SNP interactions on the risk of venous thrombosis. 23509962 2013