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
rs113488022 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490
rs121913377 0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
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
rs1042522 0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs759834365 0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237
rs1131691014 0.439 0.800 17 7676154 frameshift variant -/C ins 214
rs878854066 0.439 0.800 17 7676153 missense variant GG/AC mnv 213
rs25487 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs1695 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188
rs1805087
MTR
0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 135
rs2010963 0.542 0.840 6 43770613 5 prime UTR variant C/G snv 0.68 82
rs28934576 0.554 0.600 17 7673802 missense variant C/A;G;T snv 4.0E-06; 1.6E-05 78
rs104894229 0.564 0.600 11 534289 missense variant C/A;G;T snv 73
rs104894230 0.564 0.600 11 534288 missense variant C/A;G;T snv 73
rs699947 0.570 0.680 6 43768652 upstream gene variant A/C;T snv 67
rs3025039 0.576 0.720 6 43784799 3 prime UTR variant C/T snv 0.13 62
rs1800566 0.576 0.680 16 69711242 missense variant G/A snv 0.25 0.21 59
rs1056836 0.581 0.680 2 38071060 missense variant G/C snv 0.51 58
rs1258159645 0.630 0.600 16 69711128 missense variant G/A snv 7.0E-06 37
rs10936599 0.637 0.600 3 169774313 synonymous variant C/T snv 0.29 0.21 32
rs78311289 0.689 0.440 4 1806162 missense variant A/C;G snv 4.0E-06 25
rs121913485 0.716 0.400 4 1804372 missense variant A/G snv 18
rs603965 0.732 0.440 11 69648142 splice region variant G/A snv 14