Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs662 0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 157
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 134
rs1333049 0.614 0.520 9 22125504 intron variant G/C snv 0.41 60
rs3742264 0.742 0.400 13 46073959 missense variant C/T snv 0.31 0.35 17