rs6940467, HCP5

N. diseases: 1
Source: GWASDB ×
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
388 1.000 0.040 6 31474360 intron variant A/G snv 0.17 0.700 1.000 1 2012 2012