Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10004195 0.790 0.320 4 38783103 upstream gene variant T/A snv 0.29 8
rs1042522 0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs1053005 0.763 0.360 17 42313892 3 prime UTR variant T/C snv 0.25 10
rs1059703 0.851 0.280 X 154013378 missense variant G/A snv 0.67 6
rs1061501 0.851 0.200 11 614864 synonymous variant C/T snv 0.83 0.85 4
rs10774625 0.763 0.320 12 111472415 intron variant A/G snv 0.66 13
rs1085308054 0.827 0.160 10 87952231 frameshift variant AT/- delins 7
rs111033243 0.827 0.400 7 107689112 missense variant T/C snv 6.1E-04 8.1E-04 5
rs1131691014 0.439 0.800 17 7676154 frameshift variant -/C ins 214
rs1133076
TG
0.925 0.080 8 133113438 missense variant G/A snv 0.48 0.56 2
rs113488022 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490
rs1143627 0.605 0.760 2 112836810 5 prime UTR variant G/A snv 0.56 47
rs11568820
VDR
0.672 0.480 12 47908762 intron variant C/T snv 0.38 27
rs11571297 0.882 0.120 2 203880280 regulatory region variant T/C snv 0.44 3
rs11611206 0.851 0.200 12 68274666 intron variant G/A snv 0.15 4
rs11675434
TPO
0.827 0.240 2 1404043 non coding transcript exon variant C/T snv 0.39 5
rs1179251 0.763 0.320 12 68251271 intron variant C/G snv 0.18 14
rs11935941 1.000 0.040 4 148731326 intron variant A/C snv 0.31 2
rs12101255 0.925 0.120 14 80984708 intron variant C/T snv 0.37 2
rs121434257 0.827 0.080 21 44289686 missense variant G/A;T snv 4.0E-05 6
rs121434569 0.581 0.520 7 55181378 missense variant C/T snv 2.8E-05 5.6E-05 70
rs121913377 0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
rs121917864 0.645 0.520 4 153704936 missense variant C/T snv 8.8E-05 9.8E-05 31
rs12492609 0.882 0.040 3 119435715 intron variant C/T snv 0.14 3
rs12507813 1.000 0.040 4 165013422 upstream gene variant G/A;C;T snv 1