NCAM2, neural cell adhesion molecule 2, 4685

N. diseases: 21; N. variants: 10
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs968910165
rs968910165
Entrez Id: 4685
Gene Symbol: NCAM2
NCAM2
CUI: C3714756
Disease:
Intellectual Disability 		0.010 GeneticVariation BEFREE SNP microarray and whole exome sequencing identified a homozygous frameshift mutation (p.L870V) in SCARF2 and predicted damaging mutations in several genes, most notably DGCR2 (p.P75L) and NCAM2 (p.S147G), both possible candidates for this child's intellectual disability. 27375131 2016
dbSNP: rs111478044
rs111478044
Entrez Id: 4685
Gene Symbol: NCAM2
NCAM2
CUI: C0919267
Disease:
ovarian neoplasm 		0.700 GeneticVariation GWASCAT Genome-wide association studies identify susceptibility loci for epithelial ovarian cancer in east Asian women. 30898391 2019
dbSNP: rs35384524
rs35384524
Entrez Id: 4685
Gene Symbol: NCAM2
NCAM2
CUI: C0019196
Disease:
Hepatitis C 		0.700 GeneticVariation GWASCAT Impact of IFNL4 Genetic Variants on Sustained Virologic Response and Viremia in Hepatitis C Virus Genotype 3 Patients. 31260374 2019
dbSNP: rs11911765
rs11911765
Entrez Id: 4685
Gene Symbol: NCAM2
NCAM2
CUI: C2985280
Disease:
Blood Protein Measurement 		C 0.700 GeneticVariation GWASCAT Genomic atlas of the human plasma proteome. 29875488 2018
dbSNP: rs232464
rs232464
Entrez Id: 4685
Gene Symbol: NCAM2
NCAM2
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: rs2826851
rs2826851
Entrez Id: 4685
Gene Symbol: NCAM2
NCAM2
CUI: C2985280
Disease:
Blood Protein Measurement 		A 0.700 GeneticVariation GWASCAT Co-regulatory networks of human serum proteins link genetics to disease. 30072576 2018
dbSNP: rs34963977
rs34963977
Entrez Id: 4685
Gene Symbol: NCAM2
NCAM2
CUI: C2985280
Disease:
Blood Protein Measurement 		T 0.700 GeneticVariation GWASCAT Genomic atlas of the human plasma proteome. 29875488 2018
dbSNP: rs529138199
rs529138199
Entrez Id: 4685
Gene Symbol: NCAM2
NCAM2
CUI: C0476089
Disease:
Endometrial Carcinoma 		C 0.700 GeneticVariation GWASCAT Identification of nine new susceptibility loci for endometrial cancer. 30093612 2018
dbSNP: rs11088859
rs11088859
Entrez Id: 4685
Gene Symbol: NCAM2
NCAM2
CUI: C0028754
Disease:
Obesity 		0.800 GeneticVariation GWASCAT A genome-wide association study on obesity and obesity-related traits. 21552555 2011
dbSNP: rs11088859
rs11088859
Entrez Id: 4685
Gene Symbol: NCAM2
NCAM2
CUI: C0028754
Disease:
Obesity 		0.800 GeneticVariation GWASDB A genome-wide association study on obesity and obesity-related traits. 21552555 2011
dbSNP: rs2826891
rs2826891
Entrez Id: 4685
Gene Symbol: NCAM2
NCAM2
CUI: C0023980
Disease:
Longevity 		0.800 GeneticVariation GWASCAT Joint influence of small-effect genetic variants on human longevity. 20834067 2010
dbSNP: rs2826891
rs2826891
Entrez Id: 4685
Gene Symbol: NCAM2
NCAM2
CUI: C0023980
Disease:
Longevity 		0.800 GeneticVariation GWASDB Joint influence of small-effect genetic variants on human longevity. 20834067 2010