Source: GWASCAT ×
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: rs9939609
rs9939609
0.559 0.720 16 53786615 intron variant T/A snv 0.41
CUI: C0018801
Disease: Heart failure
Heart failure
Cardiovascular Diseases 0.700 1.000 1 2016 2016