Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs79184941 0.617 0.600 10 121520163 missense variant G/A;C snv 5.6E-05; 4.0E-06 41
rs77543610 0.667 0.560 10 121520160 missense variant G/C snv 28
rs121918487 0.716 0.440 10 121517378 missense variant C/A;G;T snv 25
rs121913478 0.708 0.640 10 121515280 missense variant T/C snv 17
rs121918491 0.716 0.440 10 121517371 synonymous variant C/T snv 4.0E-06 15
rs1554927408 0.742 0.480 10 121515254 missense variant C/T snv 12
rs1057519044 0.752 0.440 10 121517390 missense variant C/T snv 11
rs1434545235 0.752 0.440 10 121565500 missense variant T/C snv 4.0E-06 11
rs121918502 0.790 0.160 10 121517351 missense variant G/C snv 9
rs121918488 0.790 0.120 10 121517379 missense variant A/C;G;T snv 7
rs28931606
POR
0.882 0.120 7 75985655 missense variant T/A snv 3
rs777142423 1.000 0.120 3 10048010 missense variant T/C snv 1.2E-05 1
rs1467767754
POR
1.000 0.120 7 75985181 missense variant T/C snv 1