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
rs1045642 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs25487 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs2910164 0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs1799782 0.474 0.800 19 43553422 missense variant G/A snv 9.5E-02 7.0E-02 151
rs1052133 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 147
rs3746444 0.514 0.760 20 34990448 mature miRNA variant A/G snv 0.20 0.19 105
rs1048943 0.533 0.720 15 74720644 missense variant T/A;C;G snv 0.11 5.9E-02 88
rs1130409 0.555 0.720 14 20456995 missense variant T/A;C;G snv 4.0E-06; 4.0E-06; 0.42 72
rs3212227 0.566 0.840 5 159315942 3 prime UTR variant T/G snv 0.26 65
rs762846821 0.614 0.320 17 7675151 missense variant C/A;T snv 8.0E-06 57
rs2274223 0.620 0.400 10 94306584 missense variant A/G snv 0.28 0.31 40
rs11568820
VDR
0.672 0.480 12 47908762 intron variant C/T snv 0.38 27
rs1131691021 0.716 0.120 17 7675097 missense variant A/C;G snv 21
rs3765524 0.724 0.320 10 94298541 missense variant C/T snv 0.27 0.31 17
rs1800372 0.752 0.240 17 7674892 synonymous variant T/A;C snv 1.3E-02 15
rs3136038 0.763 0.200 16 13919522 upstream gene variant C/T snv 0.36 13
rs61748181 0.827 0.120 5 1294051 missense variant C/T snv 2.2E-02 2.2E-02 10
rs1989969
VDR
0.827 0.120 12 47884227 intron variant A/C;G;T snv 0.60 8
rs2228059 0.882 0.080 10 5960405 missense variant T/G snv 0.51 0.55 5