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
rs1800562 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 262
rs6265 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs1799945 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 226
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
rs854560 0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 113
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
rs6313 0.562 0.640 13 46895805 synonymous variant G/A snv 0.41 0.40 82
rs6280 0.602 0.520 3 114171968 missense variant C/T snv 0.63 0.54 57
rs1979277 0.620 0.560 17 18328782 missense variant G/A snv 0.27 0.31 45
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
rs11568820
VDR
0.672 0.480 12 47908762 intron variant C/T snv 0.38 27
rs6314 0.677 0.360 13 46834899 missense variant G/A snv 7.9E-02 9.5E-02 23
rs886040971 0.683 0.280 8 115604339 stop gained G/A;T snv 56
rs113871094 0.683 0.320 15 48465820 stop gained G/A snv 34
rs80338945 0.695 0.440 13 20189313 missense variant A/G snv 6.4E-04 6.4E-04 32
rs1006737 0.695 0.120 12 2236129 intron variant G/A snv 0.36 27
rs398124401 0.695 0.480 4 55346393 stop gained G/A snv 1.2E-04 2.8E-05 26
rs1331463984 0.701 0.240 16 2176350 missense variant G/A snv 33
rs2254298 0.701 0.200 3 8760542 intron variant G/A snv 0.16 23
rs1344706 0.701 0.160 2 184913701 intron variant A/C;T snv 21