Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800562 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 262
rs780094 0.658 0.400 2 27518370 intron variant T/C snv 0.67 62
rs7412 0.641 0.640 19 44908822 missense variant C/T snv 6.2E-02 7.9E-02 47
rs964184 0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 47
rs405509 0.667 0.480 19 44905579 upstream gene variant T/G snv 0.58 30
rs3764261 0.732 0.280 16 56959412 upstream gene variant C/A snv 0.31 26
rs1535 0.752 0.240 11 61830500 intron variant A/G snv 0.31 24
rs102275 0.827 0.320 11 61790331 non coding transcript exon variant T/C snv 0.47 18
rs174546 0.807 0.200 11 61802358 3 prime UTR variant C/T snv 0.28 17
rs673548 0.925 0.120 2 21014672 intron variant G/A;T snv 14
rs6589566 0.882 0.080 11 116781707 intron variant G/A;C;T snv 10
rs9987289 1.000 0.040 8 9325848 non coding transcript exon variant A/G snv 0.87 10
rs769450 0.925 0.120 19 44907187 non coding transcript exon variant G/A snv 0.39 5
rs7575840 1.000 0.040 2 21050618 intergenic variant G/T snv 0.26 4