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
rs1801133 0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 174
rs1805087
MTR
0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 135
rs1801131 0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 93
rs1136410 0.559 0.760 1 226367601 missense variant A/G snv 0.21 0.15 70
rs2477686 0.807 0.040 1 2461209 intron variant G/C snv 0.64 7
rs55763075 0.827 0.120 1 11790377 3 prime UTR variant C/T snv 2.1E-05 6
rs12097821 0.882 0.040 1 106793679 regulatory region variant G/A;T snv 4
rs11204546 0.925 0.040 1 247896410 missense variant T/C;G snv 0.58; 4.0E-06 3
rs777772044 1.000 0.160 1 155186160 missense variant A/C;G snv 1.5E-05 2
rs1056836 0.581 0.680 2 38071060 missense variant G/C snv 0.51 58
rs6166 0.708 0.240 2 48962782 missense variant C/T snv 0.57 0.57 17
rs6165 0.724 0.160 2 48963902 missense variant C/G;T snv 4.0E-06; 0.55 14
rs1550117 0.790 0.320 2 25343038 upstream gene variant A/G;T snv 11
rs200750564 0.827 0.160 2 176094518 stop gained C/T snv 8.0E-06 7.0E-06 6
rs1394205 0.925 0.120 2 49154446 5 prime UTR variant C/T snv 0.32 0.28 3
rs68073206 1.000 0.040 2 48721568 3 prime UTR variant A/C snv 0.29 2
rs1050482 2 112663757 3 prime UTR variant G/A snv 1
rs1399645 2 139390262 intergenic variant C/T snv 9.0E-02 1
rs140027779 2 197756444 missense variant T/C snv 8.0E-06 7.0E-06 1
rs372015936 2 197743089 missense variant G/A;C snv 4.1E-05; 4.1E-06 1
rs1052133 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 147
rs1800734 0.653 0.400 3 36993455 5 prime UTR variant G/A snv 0.22 30
rs121918346 0.882 0.040 3 16598169 missense variant T/C;G snv 8.0E-06 5