Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1131691014 0.439 0.800 17 7676154 frameshift variant -/C ins 214
rs28360317 0.716 0.280 5 83323739 intron variant -/CCT delins 0.24 15
rs712 0.677 0.360 12 25209618 3 prime UTR variant A/C snv 0.46 24
rs17879961 0.597 0.480 22 28725099 missense variant A/C;G snv 4.1E-03 53
rs113488022 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490
rs1799977 0.662 0.440 3 37012077 missense variant A/C;G;T snv 0.23 28
rs1447295 0.658 0.400 8 127472793 intron variant A/C;T snv 29
rs2032582 0.538 0.800 7 87531302 missense variant A/C;T snv 0.54; 3.8E-02 97
rs2273535 0.645 0.360 20 56386485 missense variant A/C;T snv 0.28 38
rs7041
GC
0.576 0.800 4 71752617 missense variant A/C;T snv 0.52; 4.0E-06 64
rs10505477 0.658 0.400 8 127395198 intron variant A/G snv 0.40 31
rs1128503 0.564 0.760 7 87550285 synonymous variant A/G snv 0.54 0.63 64
rs1136410 0.559 0.760 1 226367601 missense variant A/G snv 0.21 0.15 70
rs11615 0.572 0.640 19 45420395 synonymous variant A/G snv 0.50 0.55 62
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs16944 0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 92
rs1695 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188
rs1801394 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 101
rs1805087
MTR
0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 135
rs2241880 0.627 0.600 2 233274722 missense variant A/G snv 0.45 0.44 37
rs2274223 0.620 0.400 10 94306584 missense variant A/G snv 0.28 0.31 40
rs2308321 0.653 0.480 10 129766800 missense variant A/G snv 9.3E-02 8.7E-02 29
rs2853669 0.649 0.320 5 1295234 upstream gene variant A/G snv 0.25 35
rs3746444 0.514 0.760 20 34990448 mature miRNA variant A/G snv 0.20 0.19 105
rs731236
VDR
0.542 0.760 12 47844974 synonymous variant A/G snv 0.33 0.34 81