Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4898 0.672 0.520 X 47585586 synonymous variant T/C snv 0.46 0.46 25
rs398122917 0.882 0.080 X 155280059 missense variant G/C snv 4.4E-05 1.1E-04 5
rs1800206 0.641 0.640 22 46218377 missense variant C/G snv 4.3E-02 4.2E-02 35
rs4819554 0.776 0.320 22 17084145 upstream gene variant G/A snv 0.84 10
rs13058338 1.000 0.040 22 37236730 intron variant T/A;G snv 4
rs1303946678 0.925 0.040 22 42126851 missense variant C/G snv 3
rs4822489 0.925 0.200 22 24437792 intron variant T/G snv 0.48 2
rs1805127 0.732 0.240 21 34449523 missense variant T/C snv 0.64 2.0E-04 17
rs1056892 0.882 0.160 21 36146408 missense variant G/A snv 0.37 0.39 6
rs3746444 0.514 0.760 20 34990448 mature miRNA variant A/G snv 0.20 0.19 105
rs911119 0.807 0.120 20 23632100 non coding transcript exon variant C/G;T snv 9
rs587782951 0.807 0.080 20 44160305 missense variant G/T snv 6
rs6026584 0.925 0.040 20 58894018 intron variant T/C snv 0.70 3
rs452159
ADA
1.000 0.040 20 44642461 intron variant G/T snv 0.28 2
rs6123837 0.925 0.040 20 58890516 synonymous variant G/A snv 0.30 2
rs3787429 1.000 0.040 20 62216348 missense variant C/G;T snv 4.5E-06; 0.45 1
rs1800437 0.827 0.160 19 45678134 missense variant G/C snv 0.18 0.17 13
rs10423928 0.807 0.200 19 45679046 intron variant T/A snv 0.19 12
rs3745297
HRC
0.790 0.120 19 49154952 missense variant A/C snv 0.41 0.38 10
rs8259
BSG
0.776 0.200 19 582927 3 prime UTR variant T/A snv 0.39 9
rs737337 0.925 0.040 19 11236817 synonymous variant T/C snv 0.15 0.20 6
rs535039125 0.851 0.040 19 41004380 missense variant C/T snv 1.1E-04 1.3E-04 5
rs200536955 0.925 0.040 19 35756980 missense variant G/A;T snv 7.0E-04 3
rs76992529
TTR
0.653 0.560 18 31598655 missense variant G/A snv 1.1E-03 4.9E-03 36
rs121918090
TTR
0.790 0.240 18 31593026 missense variant G/C snv 8