Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs10757272
rs10757272
0.851 0.160 9 22088261 intron variant C/T snv 0.41
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.700 1.000 1 2013 2013