Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1057518083 0.851 0.120 14 101986552 missense variant C/T snv 21
rs362569 1.000 0.040 20 10266085 intron variant T/C snv 0.38 1
rs227283 0.925 0.120 4 102686096 intron variant C/G;T snv 2
rs6108461 1.000 0.040 20 10286622 intron variant A/G snv 0.57 1
rs362549 1.000 0.040 20 10289242 intron variant A/G snv 0.56 1
rs11191454 0.776 0.160 10 102900247 intron variant A/G snv 7.9E-02 9
rs362990 1.000 0.040 20 10295573 intron variant A/T snv 0.23 1
rs362998 1.000 0.040 20 10296973 synonymous variant C/T snv 0.11 0.11 1
rs7914558 0.851 0.040 10 103016151 intron variant G/A snv 0.40 5
rs3746544 0.790 0.120 20 10306436 3 prime UTR variant G/T snv 0.68 10
rs1051312 0.827 0.120 20 10306440 3 prime UTR variant T/C snv 0.20 5
rs8636 1.000 0.040 20 10307094 3 prime UTR variant T/A;C snv 1
rs11191580 0.827 0.040 10 103146454 intron variant T/C snv 7.9E-02 13
rs736707 0.851 0.040 7 103489956 intron variant A/G snv 0.30 6
rs7341475 0.851 0.240 7 103764368 intron variant G/A snv 0.17 6
rs1592757 1.000 0.040 5 104554297 intron variant G/C snv 0.29 1
rs325485 0.925 0.120 5 104659667 intron variant A/G snv 0.65 2
rs11591402 1.000 0.040 10 104987596 intron variant T/A;G snv 1
rs9297357 0.851 0.040 8 105130105 intron variant C/G;T snv 5
rs11074889 1.000 0.040 16 10539308 intron variant A/G;T snv 1
rs6539247 1.000 0.040 12 106066124 3 prime UTR variant T/C;G snv 1
rs2230460 0.925 0.040 7 106884244 synonymous variant C/T snv 0.12 8.5E-02 2
rs12536620 1.000 0.040 7 106904783 intron variant A/G snv 0.42 1
rs12667819 1.000 0.040 7 106906212 3 prime UTR variant G/A snv 0.41 1
rs12871532 0.851 0.040 13 108016199 intergenic variant T/C snv 0.46 5