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: 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: rs1816537
rs1816537
Entrez Id: 4684
Gene Symbol: NCAM1
NCAM1
CUI: C1305855
Disease:
Body mass index
A 0.700 GeneticVariation GWASCAT A Large Multiethnic Genome-Wide Association Study of Adult Body Mass Index Identifies Novel Loci. 30108127 2018
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: 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
dbSNP: rs10891483
rs10891483
Entrez Id: 4684
Gene Symbol: NCAM1
NCAM1
CUI: C0205682
Disease:
Waist-Hip Ratio
T 0.700 GeneticVariation GWASCAT Association of Genetic Variants Related to Gluteofemoral vs Abdominal Fat Distribution With Type 2 Diabetes, Coronary Disease, and Cardiovascular Risk Factors. 30575882 2018
dbSNP: rs2288158
rs2288158
Entrez Id: 4684
Gene Symbol: NCAM1
NCAM1
CUI: C2985280
Disease:
Blood Protein Measurement
T 0.700 GeneticVariation GWASCAT Co-regulatory networks of human serum proteins link genetics to disease. 30072576 2018
dbSNP: rs2155292
rs2155292
Entrez Id: 4684
Gene Symbol: NCAM1
NCAM1
CUI: C0596887
Disease:
mathematical ability
A 0.700 GeneticVariation GWASCAT Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals. 30038396 2018
dbSNP: rs3802850
rs3802850
Entrez Id: 4684
Gene Symbol: NCAM1
NCAM1
CUI: C0596887
Disease:
mathematical ability
A 0.700 GeneticVariation GWASCAT Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals. 30038396 2018
dbSNP: rs7111153
rs7111153
Entrez Id: 4684;101928847
Gene Symbol: NCAM1;LOC101928847
NCAM1;LOC101928847
CUI: C0596887
Disease:
mathematical ability
T 0.700 GeneticVariation GWASCAT Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals. 30038396 2018
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: 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: rs61902492
rs61902492
Entrez Id: 4684
Gene Symbol: NCAM1
NCAM1
CUI: C0037369
Disease:
Smoking
A 0.700 GeneticVariation GWASCAT Genome-wide association analyses of risk tolerance and risky behaviors in over 1 million individuals identify hundreds of loci and shared genetic influences. 30643258 2019
dbSNP: rs7938812
rs7938812
Entrez Id: 4684
Gene Symbol: NCAM1
NCAM1
CUI: C0037369
Disease:
Smoking
T 0.700 GeneticVariation GWASCAT Genome-wide association analyses of risk tolerance and risky behaviors in over 1 million individuals identify hundreds of loci and shared genetic influences. 30643258 2019
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: rs2885208
rs2885208
Entrez Id: 4684
Gene Symbol: NCAM1
NCAM1
CUI: C0021704
Disease:
Intelligence
T 0.700 GeneticVariation GWASCAT Genome-wide association meta-analysis in 269,867 individuals identifies new genetic and functional links to intelligence. 29942086 2018
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: 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: 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: rs11214489
rs11214489
Entrez Id: 4684
Gene Symbol: NCAM1
NCAM1
CUI: C2985280
Disease:
Blood Protein Measurement
C 0.700 GeneticVariation GWASCAT Genome-wide mapping of plasma protein QTLs identifies putatively causal genes and pathways for cardiovascular disease. 30111768 2018
dbSNP: rs1273044
rs1273044
Entrez Id: 4684
Gene Symbol: NCAM1
NCAM1
CUI: C2985280
Disease:
Blood Protein Measurement
C 0.700 GeneticVariation GWASCAT Genomic atlas of the human plasma proteome. 29875488 2018
dbSNP: rs78599561
rs78599561
Entrez Id: 4684
Gene Symbol: NCAM1
NCAM1
CUI: C2985280
Disease:
Blood Protein Measurement
A 0.700 GeneticVariation GWASCAT Genomic atlas of the human plasma proteome. 29875488 2018