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: 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
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: 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