CNTN5, contactin 5, 53942

N. diseases: 34; N. variants: 20
Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs10501920
rs10501920
0.882 0.080 11 99622442 intron variant C/G snv 0.14
CUI: C0018801
Disease: Heart failure
Heart failure
Cardiovascular Diseases 0.010 1.000 1 2007 2007