Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs6265 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs4680 0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs759834365 0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237
rs1801133 0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 174
rs662 0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 157
rs1805087
MTR
0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 135
rs1801394 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 101
rs1799971 0.559 0.600 6 154039662 missense variant A/G snv 0.19 0.12 95
rs25531 0.581 0.520 17 30237328 upstream gene variant T/C snv 0.18 72
rs1800497 0.620 0.400 11 113400106 missense variant G/A snv 0.26 0.26 56
rs4588
GC
0.597 0.720 4 71752606 missense variant G/A;T snv 1.6E-05; 0.25 53
rs53576 0.641 0.320 3 8762685 intron variant A/G;T snv 42
rs6311 0.645 0.640 13 46897343 upstream gene variant C/T snv 0.40 41
rs2254298 0.701 0.200 3 8760542 intron variant G/A snv 0.16 23
rs6314 0.677 0.360 13 46834899 missense variant G/A snv 7.9E-02 9.5E-02 23
rs893924483 0.716 0.280 11 27658285 missense variant C/A;T snv 4.0E-06 1.4E-05 23
rs4906902 0.724 0.200 15 26774621 intron variant A/G snv 0.15 14
rs397514679 0.790 0.200 X 47574321 stop gained G/A snv 9
rs3796863 0.790 0.160 4 15848363 intron variant G/T snv 0.41 8
rs2268498 0.827 0.080 3 8770725 intron variant T/C snv 0.41 7
rs561077 0.882 0.080 X 151181177 missense variant A/G snv 0.43 0.45 4