Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1805087
MTR
0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 135
rs4880 0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 131
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
rs16944 0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 92
rs4994 0.578 0.640 8 37966280 missense variant A/G snv 0.11 9.2E-02 65
rs9340799 0.583 0.680 6 151842246 intron variant A/G snv 0.32 62
rs2075650 0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 45
rs1799889 0.649 0.600 7 101126430 upstream gene variant A/G snv 31
rs1801260 0.695 0.280 4 55435202 3 prime UTR variant A/G snv 0.25 28
rs334558 0.701 0.320 3 120094435 upstream gene variant A/G snv 0.51 20
rs10434 0.701 0.480 6 43785475 3 prime UTR variant A/G snv 0.59 17
rs2230912 0.752 0.280 12 121184393 missense variant A/G snv 0.13 0.12 16
rs9296158 0.763 0.080 6 35599305 intron variant A/G snv 0.65 16
rs4906902 0.724 0.200 15 26774621 intron variant A/G snv 0.15 14
rs2227631 0.742 0.200 7 101126257 upstream gene variant A/G snv 0.54 13
rs11030104 0.790 0.240 11 27662970 intron variant A/G snv 0.16 12
rs7997012 0.807 0.080 13 46837850 intron variant A/G snv 0.69 11
rs900418273 0.807 0.120 11 113393764 missense variant A/G snv 8
rs139315125 0.851 0.080 1 7809900 missense variant A/G snv 5.6E-03 5.0E-03 7
rs4795541 0.807 0.200 17 30237299 upstream gene variant A/G snv 7
rs1013940 0.827 0.160 2 107992192 missense variant A/G snv 9.3E-02 7.4E-02 6
rs1409851868 0.882 0.080 3 89399325 missense variant A/G snv 6
rs2253206 0.851 0.080 2 207527254 intron variant A/G snv 0.47 6
rs3789327 0.925 0.080 11 13363769 intron variant A/G snv 0.53 6