Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs942158624 0.724 0.320 17 7674948 missense variant T/A snv 19
rs878854066 0.439 0.800 17 7676153 missense variant GG/AC mnv 213
rs869320694 0.742 0.520 8 38414790 missense variant T/C snv 16
rs861539 0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 104
rs78378222 0.662 0.360 17 7668434 3 prime UTR variant T/G snv 8.3E-03 37
rs758272654 0.611 0.680 20 58909201 synonymous variant T/C snv 4.0E-06 7.0E-06 50
rs7003908 0.716 0.320 8 47858141 intron variant C/A snv 0.66 16
rs6010620 0.701 0.360 20 63678486 intron variant A/C;G snv 21
rs587778720 0.667 0.360 17 7674893 missense variant C/A;G;T snv 4.0E-06 31
rs55819519 0.627 0.400 17 7673751 missense variant C/A;G;T snv 1.6E-04 1.3E-04 40
rs55705857 0.732 0.080 8 129633446 intron variant A/G snv 3.9E-02 16
rs3856806 0.637 0.440 3 12434058 synonymous variant C/T snv 0.13 0.11 41
rs28934578 0.605 0.600 17 7675088 missense variant C/A;T snv 4.0E-06 47
rs28934576 0.554 0.600 17 7673802 missense variant C/A;G;T snv 4.0E-06; 1.6E-05 78
rs28934575 0.641 0.400 17 7674230 missense variant C/A;G;T snv 37
rs28934574 0.658 0.440 17 7673776 missense variant G/A;C snv 4.0E-06 31
rs28934573 0.667 0.480 17 7674241 missense variant G/A;C;T snv 4.0E-06 28
rs2853669 0.649 0.320 5 1295234 upstream gene variant A/G snv 0.25 35
rs2736100 0.550 0.880 5 1286401 3 prime UTR variant C/A snv 0.52 83
rs2736098 0.600 0.600 5 1293971 synonymous variant C/T snv 0.29 0.22 48
rs25487 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs20541 0.585 0.720 5 132660272 missense variant A/G snv 0.72 0.77 52
rs2010963 0.542 0.840 6 43770613 5 prime UTR variant C/G snv 0.68 82
rs1805087
MTR
0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 135
rs1805015 0.683 0.520 16 27362859 missense variant T/C snv 0.16 0.22 22