Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7741604 0.925 0.120 6 20731293 intron variant A/C;T snv 2
rs16859788 1.000 0.040 4 46969992 intron variant A/C;T snv 1
rs971257 1.000 0.040 2 167782126 intergenic variant A/C;T snv 0.53 1
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1805087
MTR
0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 135
rs1801394 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 101
rs1799971 0.559 0.600 6 154039662 missense variant A/G snv 0.19 0.12 95
rs80338945 0.695 0.440 13 20189313 missense variant A/G snv 6.4E-04 6.4E-04 32
rs148881970 0.724 0.360 17 42543840 missense variant A/G snv 5.4E-05 1.3E-04 22
rs1060499733 0.851 0.120 3 47846757 missense variant A/G snv 11
rs11191454 0.776 0.160 10 102900247 intron variant A/G snv 7.9E-02 9
rs736707 0.851 0.040 7 103489956 intron variant A/G snv 0.30 6
rs12456492 0.882 0.080 18 43093415 intron variant A/G snv 0.33 3
rs155806 1.000 0.040 5 140970255 intron variant A/G snv 8.9E-02 2
rs753426385 0.925 0.120 Y 14840846 missense variant A/G snv 2
rs879254129 0.925 0.040 12 13562977 missense variant A/G snv 4.0E-06 2
rs9635542
PPL
1.000 0.040 16 4951379 intron variant A/G snv 0.11 2
rs10500171 1.000 0.040 7 147183313 intron variant A/G snv 0.52 1
rs1057518999 1.000 0.040 3 70977826 splice donor variant A/G snv 1
rs10732392 1.000 0.040 9 126633758 intron variant A/G snv 0.84 1
rs11102807 1.000 0.040 1 114518963 intergenic variant A/G snv 0.44 1
rs12336217 1.000 0.040 9 126637591 intron variant A/G snv 0.17 1
rs12518194 1.000 0.040 5 25951452 intergenic variant A/G snv 0.27 1
rs1408744 1.000 0.040 6 23789887 intergenic variant A/G snv 0.63 1
rs1426217 1.000 0.040 15 26575978 intron variant A/G snv 0.46 1