Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121434592 0.595 0.640 14 104780214 missense variant C/T snv 4.0E-06 54
rs17655 0.597 0.560 13 102875652 missense variant G/C snv 0.28 0.30 52
rs113488022 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490
rs121913227 0.653 0.320 7 140753336 missense variant AC/CT;TT mnv 31
rs121913338 0.677 0.400 7 140753354 missense variant T/A;C;G snv 24
rs121913348 0.763 0.480 7 140781617 missense variant C/A;G;T snv 20
rs121913351 0.776 0.240 7 140781611 missense variant C/A;G;T snv 4.0E-06 9
rs121913355 0.641 0.520 7 140781602 missense variant C/A;G;T snv 4.0E-06 42
rs121913357 0.742 0.320 7 140781603 stop gained C/A;G;T snv 12
rs121913364 0.641 0.520 7 140753334 missense variant T/C;G snv 4.0E-06 34
rs121913369 0.790 0.280 7 140753346 missense variant G/A;C snv 4.0E-06 12
rs121913370 0.763 0.360 7 140753393 missense variant T/C;G snv 10
rs121913377 0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
rs121913378 0.776 0.280 7 140753337 missense variant C/A;G;T snv 11
rs397516896 0.763 0.360 7 140753355 missense variant C/G;T snv 11
rs121913386 0.807 0.120 9 21971018 missense variant G/A;T snv 7
rs401681 0.620 0.640 5 1321972 intron variant C/T snv 0.48 42
rs121913409 0.708 0.400 3 41224646 missense variant C/A;G;T snv 21
rs397517132 0.623 0.280 7 55191846 missense variant A/T snv 48
rs121434569 0.581 0.520 7 55181378 missense variant C/T snv 2.8E-05 5.6E-05 70
rs1799793 0.557 0.640 19 45364001 missense variant C/A;T snv 7.1E-06; 0.29 72
rs7041
GC
0.576 0.800 4 71752617 missense variant A/C;T snv 0.52; 4.0E-06 64
rs758272654 0.611 0.680 20 58909201 synonymous variant T/C snv 4.0E-06 7.0E-06 50
rs1138272 0.611 0.600 11 67586108 missense variant C/T snv 5.9E-02 5.5E-02 42
rs1695 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188