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
rs1799945 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 226
rs1801133 0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 174
rs1052133 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 147
rs1800795 0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs1805087
MTR
0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 135
rs34637584 0.583 0.480 12 40340400 missense variant G/A snv 5.3E-04 3.6E-04 78
rs1130409 0.555 0.720 14 20456995 missense variant T/A;C;G snv 4.0E-06; 4.0E-06; 0.42 72
rs1024611 0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28 63
rs104893877 0.614 0.360 4 89828149 missense variant C/T snv 59
rs121912438 0.605 0.520 21 31667299 missense variant G/A;C;T snv 1.2E-05; 8.0E-06 58
rs775144154 0.627 0.600 21 45531904 missense variant C/A;T snv 9.7E-06; 1.4E-05 38
rs368087026 0.637 0.520 21 45530890 missense variant G/A snv 33
rs1448674651 0.667 0.560 18 671384 missense variant G/A;C snv 4.0E-06 23
rs104893878 0.732 0.160 4 89835580 missense variant C/G snv 21
rs121912443 0.732 0.160 21 31663857 missense variant A/G snv 15
rs367543041 0.742 0.200 1 11022553 missense variant G/A;C snv 3.0E-05 15
rs1481318368
TH
0.827 0.120 11 2169802 missense variant C/T snv 10
rs35870237 0.763 0.120 12 40340404 missense variant T/C snv 9
rs774005786 0.790 0.080 1 7970951 missense variant G/A;T snv 3.9E-04; 2.0E-05 8
rs28938172 0.790 0.080 1 7984981 missense variant T/C snv 7
rs34995376 0.807 0.080 12 40310435 missense variant G/A snv 7.0E-06 7
rs74315355 0.790 0.080 1 20644639 missense variant G/A snv 7