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
rs1805087
MTR
0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 135
rs5361 0.623 0.720 1 169731919 missense variant T/G snv 8.3E-02; 8.0E-06 7.8E-02 47
rs1458766475 0.637 0.680 1 169732649 missense variant C/G;T snv 4.0E-06; 4.0E-06 41
rs34612342 0.653 0.400 1 45332803 missense variant T/C snv 1.5E-03 1.6E-03 32
rs486907 0.667 0.360 1 182585422 missense variant C/T snv 0.31 0.28 32
rs74315364 0.732 0.200 1 182586014 stop gained C/A snv 3.6E-03; 4.0E-06 3.3E-03 13
rs1194611372 0.763 0.320 1 152032679 missense variant A/C snv 9
rs1037189404 0.776 0.280 1 155187519 missense variant C/T snv 8
rs766333007 0.776 0.280 1 155192274 missense variant C/T snv 7.0E-06 8
rs3790843 0.827 0.160 1 200041696 intron variant C/T snv 0.29 7
rs3790844 0.882 0.200 1 200038304 intron variant A/C;G snv 4
rs78303930
NES
0.925 0.120 1 156670593 missense variant C/A;G snv 4.0E-06; 2.4E-03 4
rs12029406 0.882 0.120 1 199936700 intergenic variant C/T snv 0.36 3
rs1209809979 0.925 0.120 1 45568989 missense variant A/G snv 4.0E-06 3
rs1034925236 0.925 0.120 1 200048258 missense variant G/C snv 2
rs10919791 0.925 0.240 1 199996040 intergenic variant G/A snv 0.22 2
rs13303010 0.925 0.120 1 959193 intron variant G/A snv 0.82 0.69 2
rs2816938 1.000 0.120 1 200016240 upstream gene variant T/A snv 0.37 2
rs747601652 0.925 0.120 1 74723233 missense variant A/G snv 1.2E-05 2
rs935821839 0.925 0.120 1 3727199 missense variant A/G snv 7.0E-06 2
rs949647240 0.925 0.120 1 3707693 missense variant C/T snv 2
rs1326889 1.000 0.120 1 230727252 intron variant C/A;T snv 1
rs16861827 1.000 0.120 1 18351676 intron variant C/T snv 0.12 1