Source: CLINVAR ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs104894229 0.564 0.600 11 534289 missense variant C/A;G;T snv 52
rs11540652 0.592 0.640 17 7674220 missense variant C/A;G;T snv 1.2E-05 42
rs28934576 0.554 0.600 17 7673802 missense variant C/A;G;T snv 4.0E-06; 1.6E-05 39
rs121912651 0.605 0.680 17 7674221 missense variant G/A;C snv 4.0E-06 37
rs104894230 0.564 0.600 11 534288 missense variant C/A;G;T snv 36
rs121913482 0.630 0.680 4 1801837 missense variant C/T snv 35
rs121913355 0.641 0.520 7 140781602 missense variant C/A;G;T snv 4.0E-06 32
rs104894228 0.605 0.560 11 534286 missense variant C/A;G;T snv 30
rs121913343 0.611 0.520 17 7673803 missense variant G/A;C;T snv 1.2E-05 29
rs11554290 0.583 0.600 1 114713908 missense variant T/A;C;G snv 25
rs104894226 0.658 0.560 11 534285 missense variant C/A;G;T snv 23
rs113488022 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 22
rs28934874 0.695 0.480 17 7675161 missense variant G/A;C;T snv 21
rs121913233 0.627 0.520 11 533874 missense variant T/A;C;G snv 20
rs1057519981 0.689 0.440 17 7674251 missense variant A/C;G;T snv 20
rs587781525 0.689 0.480 17 7673778 missense variant T/A;C;G snv 20
rs730882005 0.701 0.400 17 7674250 missense variant C/A;G;T snv 8.0E-06 20
rs764146326 0.662 0.480 17 7673779 missense variant C/A;G;T snv 4.0E-06 20
rs121913529 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 19
rs121913255 0.667 0.400 1 114713907 missense variant T/A;G snv 19
rs863224451 0.701 0.440 17 7673796 missense variant C/A;G;T snv 19
rs121913500 0.529 0.600 2 208248388 missense variant C/A;G;T snv 4.0E-06 18
rs760043106 0.645 0.440 17 7674947 missense variant A/C;G;T snv 18
rs28933406 0.667 0.480 11 533875 missense variant G/C;T snv 17
rs1057520007 0.701 0.440 17 7674917 missense variant T/A;C;G snv 17