NCAM1, neural cell adhesion molecule 1, 4684

N. diseases: 445; N. variants: 34
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs5794844
rs5794844
Entrez Id: 4684
Gene Symbol: NCAM1
NCAM1
CUI: C0871470
Disease:
Systolic Pressure 		GT 0.700 GeneticVariation GWASCAT Genome-wide association analyses using electronic health records identify new loci influencing blood pressure variation. 27841878 2017
dbSNP: rs668204
rs668204
Entrez Id: 4684
Gene Symbol: NCAM1
NCAM1
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: rs4471463
rs4471463
Entrez Id: 4684
Gene Symbol: NCAM1
NCAM1
CUI: C3160814
Disease:
Cannabis use 		T 0.700 GeneticVariation GWASCAT Genome-wide association study of lifetime cannabis use based on a large meta-analytic sample of 32 330 subjects from the International Cannabis Consortium. 27023175 2016
dbSNP: rs1816537
rs1816537
Entrez Id: 4684
Gene Symbol: NCAM1
NCAM1
CUI: C1305855
Disease:
Body mass index 		C 0.700 GeneticVariation GWASCAT Genetic studies of body mass index yield new insights for obesity biology. 25673413 2015
dbSNP: rs1816537
rs1816537
Entrez Id: 4684
Gene Symbol: NCAM1
NCAM1
CUI: C1305855
Disease:
Body mass index 		A 0.700 GeneticVariation GWASCAT The Influence of Age and Sex on Genetic Associations with Adult Body Size and Shape: A Large-Scale Genome-Wide Interaction Study. 26426971 2015
dbSNP: rs1940700
rs1940700
Entrez Id: 4684
Gene Symbol: NCAM1
NCAM1
CUI: C0392885
Disease:
High density lipoprotein measurement 		0.700 GeneticVariation GWASDB Large-scale gene-centric meta-analysis across 32 studies identifies multiple lipid loci. 23063622 2012
dbSNP: rs1940700
rs1940700
Entrez Id: 4684
Gene Symbol: NCAM1
NCAM1
CUI: C0428472
Disease:
Serum HDL cholesterol measurement 		0.700 GeneticVariation GWASDB Large-scale gene-centric meta-analysis across 32 studies identifies multiple lipid loci. 23063622 2012
dbSNP: rs2155287
rs2155287
Entrez Id: 4684
Gene Symbol: NCAM1
NCAM1
CUI: C0523465
Disease:
Serum albumin measurement 		0.700 GeneticVariation GWASDB Genome-wide association study identifies multiple loci influencing human serum metabolite levels. 22286219 2012
dbSNP: rs643830
rs643830
Entrez Id: 4684
Gene Symbol: NCAM1
NCAM1
CUI: C0392885
Disease:
High density lipoprotein measurement 		0.700 GeneticVariation GWASDB Large-scale gene-centric meta-analysis across 32 studies identifies multiple lipid loci. 23063622 2012
dbSNP: rs643830
rs643830
Entrez Id: 4684
Gene Symbol: NCAM1
NCAM1
CUI: C0428472
Disease:
Serum HDL cholesterol measurement 		0.700 GeneticVariation GWASDB Large-scale gene-centric meta-analysis across 32 studies identifies multiple lipid loci. 23063622 2012
dbSNP: rs1436109
rs1436109
Entrez Id: 4684
Gene Symbol: NCAM1
NCAM1
CUI: C0011904
Disease:
Diagnostic Techniques, Cardiovascular 		0.700 GeneticVariation GWASCAT Genetic variation in NCAM1 contributes to left ventricular wall thickness in hypertensive families. 21212386 2011
dbSNP: rs1436109
rs1436109
Entrez Id: 4684
Gene Symbol: NCAM1
NCAM1
CUI: C0455825
Disease:
Left ventricular mass 		0.700 GeneticVariation GWASDB Genetic variation in NCAM1 contributes to left ventricular wall thickness in hypertensive families. 21212386 2011
dbSNP: rs1436109
rs1436109
Entrez Id: 4684
Gene Symbol: NCAM1
NCAM1
CUI: C0149721
Disease:
Left Ventricular Hypertrophy 		0.700 GeneticVariation GWASCAT Genetic variation in NCAM1 contributes to left ventricular wall thickness in hypertensive families. 21212386 2011
dbSNP: rs782464336
rs782464336
Entrez Id: 4684;100288346
Gene Symbol: NCAM1;NCAM1-AS1
NCAM1;NCAM1-AS1
CUI: C0023467
Disease:
Leukemia, Myelocytic, Acute 		0.010 GeneticVariation BEFREE In AML cohort of 239 patients, high IL2RA mRNA expression independently predicted shorter relapse free survival (RFS, p < 0.001) and overall survival (OS, p < 0.001) irrespective of age, cytogenetics, FLT3-ITD or c-KIT D816V mutational status. 31171000 2019
dbSNP: rs2301228
rs2301228
Entrez Id: 4684;101928847
Gene Symbol: NCAM1;LOC101928847
NCAM1;LOC101928847
CUI: C0036341
Disease:
Schizophrenia 		0.010 GeneticVariation BEFREE A promoter variant, rs2301228, was found to be associated with schizophrenia at the allelic level and was validated in a replication cohort. 25445624 2014
dbSNP: rs4492854
rs4492854
Entrez Id: 4684
Gene Symbol: NCAM1
NCAM1
CUI: C0019337
Disease:
Heroin Dependence 		0.010 GeneticVariation BEFREE Aggregate heroin dependence risk associated with 2 SNPs, rs877138 and rs4492854 (located in NCAM1), varied more than 4-fold (P = 2.7 × 10(-9) for the risk-associated linear trend). 23303482 2013
dbSNP: rs2303377
rs2303377
Entrez Id: 4684
Gene Symbol: NCAM1
NCAM1
CUI: C0036341
Disease:
Schizophrenia 		0.010 GeneticVariation BEFREE A genotypic association between bipolar disorder and SNP b (rs2303377 near mini-exon b) and a suggestive association between schizophrenia and SNP 9 (rs646558) were found. 17413444 2007
dbSNP: rs646558
rs646558
Entrez Id: 4684
Gene Symbol: NCAM1
NCAM1
CUI: C0036341
Disease:
Schizophrenia 		0.010 GeneticVariation BEFREE A genotypic association between bipolar disorder and SNP b (rs2303377 near mini-exon b) and a suggestive association between schizophrenia and SNP 9 (rs646558) were found. 17413444 2007
dbSNP: rs2298526
rs2298526
Entrez Id: 4684
Gene Symbol: NCAM1
NCAM1
CUI: C0027794
Disease:
Neural Tube Defects 		0.010 GeneticVariation BEFREE Association analysis revealed a significant association between risk for NTDs and intronic SNP rs2298526 using both the FBAT test (P=0.0018) and the PDT (P=0.0025). 15883837 2005