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
rs1137101 0.554 0.760 1 65592830 missense variant A/G snv 0.51 0.50 77
rs486907 0.667 0.360 1 182585422 missense variant C/T snv 0.31 0.28 32
rs646776 0.752 0.240 1 109275908 downstream gene variant C/T snv 0.74 25
rs1047840 0.708 0.280 1 241878999 missense variant G/A snv 0.36 0.40 19
rs11206510 0.763 0.240 1 55030366 intergenic variant T/A;C;G snv 16
rs1256046734 0.763 0.280 1 65621409 missense variant A/G snv 7.0E-06 12
rs17568 0.752 0.320 1 1212042 synonymous variant C/T snv 0.37 0.31 12
rs1194611372 0.763 0.320 1 152032679 missense variant A/C snv 9
rs4645978 0.827 0.120 1 15525539 intron variant C/A;T snv 8
rs1454328441 0.827 0.200 1 155192002 missense variant G/A;T snv 4.6E-06; 9.1E-06 6
rs201701502 0.851 0.080 1 162775837 missense variant C/G;T snv 1.5E-04 2.1E-05 5
rs2273953 0.851 0.120 1 3682336 5 prime UTR variant G/A;T snv 0.20; 3.3E-04 5
rs765660823 0.882 0.200 1 162778720 missense variant A/C snv 1.9E-04 4
rs144594252 0.882 0.080 1 162754625 missense variant C/G snv 6.8E-05 5.6E-05 3
rs267598140 0.925 0.080 1 162778600 missense variant T/A;G snv 3
rs1047325 1.000 0.040 1 153561551 missense variant C/T snv 7.1E-02 0.16 2
rs115169993 1.000 0.040 1 162772032 missense variant G/A snv 7.8E-04 2.9E-03 1
rs2298211 1.000 0.040 1 1211863 intron variant A/C snv 8.1E-02 8.2E-02 1
rs532172691 1.000 0.040 1 153563811 stop gained G/A snv 2.2E-04 3.4E-04 1
rs4299376 0.851 0.120 2 43845437 intron variant G/C;T snv 11
rs3087386 0.790 0.160 2 99439044 missense variant A/G snv 0.58 0.61 8
rs3087399 0.882 0.120 2 99438696 missense variant T/C snv 0.13 0.17 4