CNTN5, contactin 5, 53942

N. diseases: 34; N. variants: 20
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs10501920
rs10501920
Entrez Id: 53942
Gene Symbol: CNTN5
CNTN5
CUI: C0018801
Disease:
Heart failure 		0.010 GeneticVariation BEFREE Also, rs10501920 in CNTN5 was associated with AF (p = 9.4 x 10(-6)) and HF (p = 1.2 x 10(-4)). 17903304 2007