Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1052501 0.925 0.160 3 41883906 missense variant C/G;T snv 0.80 2
rs25487 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs1042522 0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs2228570
VDR
0.521 0.760 12 47879112 start lost A/C;G;T snv 0.63 98
rs2032582 0.538 0.800 7 87531302 missense variant A/C;T snv 0.54; 3.8E-02 97
rs1128503 0.564 0.760 7 87550285 synonymous variant A/G snv 0.54 0.63 64
rs2235544 0.742 0.240 1 53909897 intron variant C/A;T snv 0.53; 4.0E-06 10
rs1884444 0.637 0.600 1 67168129 missense variant G/T snv 0.52 0.51 34
rs1045642 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs1801274 0.597 0.800 1 161509955 missense variant A/C;G snv 4.0E-06; 0.48 41
rs1049623 0.925 0.200 6 30897052 synonymous variant T/C snv 0.47 0.43 2
rs1801394 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 101
rs9344 0.653 0.480 11 69648142 splice region variant G/A snv 0.45 0.39 30
rs12717 0.925 0.160 6 170553212 missense variant G/C snv 0.42 0.38 2
rs6465657 0.807 0.280 7 98187015 intron variant C/T snv 0.41 0.37 4
rs2302777 0.925 0.200 17 40023239 synonymous variant A/G snv 0.39 0.30 1
rs2228145 0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 48
rs1695 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 187
rs2834167 0.752 0.360 21 33268483 missense variant A/G snv 0.33 0.25 10
rs2043211 0.653 0.480 19 48234449 missense variant A/T snv 0.33 0.29 29
rs10936599 0.637 0.600 3 169774313 synonymous variant C/T snv 0.29 0.21 18
rs7853346 0.851 0.200 9 33676096 non coding transcript exon variant C/G snv 0.28; 1.2E-05 0.32 6
rs3815768 1.000 0.160 5 95900755 missense variant C/T snv 0.27 0.29 1
rs1800566 0.576 0.680 16 69711242 missense variant G/A snv 0.25 0.21 59
rs1805087
MTR
0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 135