Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1042522 0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs1130409 0.555 0.720 14 20456995 missense variant T/A;C;G snv 4.0E-06; 4.0E-06; 0.42 72
rs1131691014 0.439 0.800 17 7676154 frameshift variant -/C ins 214
rs121434592 0.595 0.640 14 104780214 missense variant C/T snv 4.0E-06 54
rs13181 0.487 0.760 19 45351661 stop gained T/A;G snv 4.0E-06; 0.32 134
rs1799793 0.557 0.640 19 45364001 missense variant C/A;T snv 7.1E-06; 0.29 72
rs1799796 0.790 0.240 14 103699590 intron variant T/A;C snv 0.31 7
rs1799983 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs1800470 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 107
rs1800471 0.597 0.840 19 41352971 missense variant C/G;T snv 5.6E-02 48
rs1805192 0.510 0.840 3 12379739 missense variant C/G snv 121
rs20417 0.576 0.600 1 186681189 non coding transcript exon variant C/G;T snv 57
rs2234922 0.630 0.440 1 225838705 missense variant A/G;T snv 0.19; 2.8E-05 42
rs2295080 0.695 0.320 1 11262571 upstream gene variant G/C;T snv 20
rs25489 0.550 0.720 19 43552260 missense variant C/G;T snv 8.5E-06; 7.1E-02 78
rs3218536 0.620 0.440 7 152648922 missense variant C/G;T snv 4.0E-06; 6.4E-02 37
rs3730358 0.724 0.360 14 104780070 intron variant G/A;C snv 0.16; 4.0E-03 14
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs699947 0.570 0.680 6 43768652 upstream gene variant A/C;T snv 67
rs763059810 0.623 0.600 2 136115750 missense variant T/C snv 4.0E-06 41
rs768623239 0.662 0.640 1 109689278 missense variant A/G snv 1.5E-05 26
rs878854066 0.439 0.800 17 7676153 missense variant GG/AC mnv 213
rs937475913 0.790 0.120 8 47936435 missense variant T/C snv 4.0E-06 7
rs953038635 0.590 0.800 6 159692720 missense variant G/A;T snv 8.0E-06 51
rs758272654 0.611 0.680 20 58909201 synonymous variant T/C snv 4.0E-06 7.0E-06 50