SHC4, SHC adaptor protein 4, 399694

N. diseases: 12; N. variants: 5
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs10162880
rs10162880
Entrez Id: 399694
Gene Symbol: SHC4
SHC4
CUI: C0523465
Disease:
Serum albumin measurement 		0.700 GeneticVariation GWASDB A genome-wide assessment of variability in human serum metabolism. 23281178 2013
dbSNP: rs10519193
rs10519193
Entrez Id: 399694
Gene Symbol: SHC4
SHC4
CUI: C0523465
Disease:
Serum albumin measurement 		0.700 GeneticVariation GWASDB A genome-wide assessment of variability in human serum metabolism. 23281178 2013
dbSNP: rs8023445
rs8023445
Entrez Id: 399694
Gene Symbol: SHC4
SHC4
CUI: C0027404
Disease:
Narcolepsy 		0.700 GeneticVariation GWASDB Genome-wide association database developed in the Japanese Integrated Database Project. 19629137 2009
dbSNP: rs11854994
rs11854994
Entrez Id: 399694
Gene Symbol: SHC4
SHC4
CUI: C0037290
Disease:
Skin Pigmentation 		0.700 GeneticVariation GWASDB A genomewide association study of skin pigmentation in a South Asian population. 17999355 2007
dbSNP: rs4774527
rs4774527
Entrez Id: 399694
Gene Symbol: SHC4
SHC4
CUI: C0037290
Disease:
Skin Pigmentation 		0.700 GeneticVariation GWASDB A genomewide association study of skin pigmentation in a South Asian population. 17999355 2007