Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10502575 18 31756628 downstream gene variant A/G snv 6.9E-02 1
rs4810479 1.000 0.040 20 45916409 upstream gene variant C/T snv 0.68 7
rs117854110 1.000 0.080 7 105603002 upstream gene variant C/A;T snv 2
rs712964 22 19168604 upstream gene variant T/C snv 0.66 2
rs749924 2 242084344 upstream gene variant C/T snv 0.25 1
rs8089491 18 31763291 upstream gene variant G/A snv 5.4E-02 1
rs1333039 1.000 0.040 9 22065658 splice region variant G/A;C;T snv 2
rs7092929 10 3496602 splice region variant A/C;T snv 1
rs964184 0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 47
rs1063192 0.695 0.520 9 22003368 3 prime UTR variant G/A;T snv 24
rs3217992 0.683 0.480 9 22003224 3 prime UTR variant C/T snv 0.32 22
rs564398 0.716 0.360 9 22029548 3 prime UTR variant T/C snv 0.31 0.28 18
rs10889332 1.000 0.120 1 62485187 3 prime UTR variant C/T snv 0.39 4
rs2657880 12 56469986 3 prime UTR variant G/C snv 0.15 4
rs102275 0.827 0.320 11 61790331 non coding transcript exon variant T/C snv 0.47 18
rs2157719 0.708 0.360 9 22033367 non coding transcript exon variant C/T snv 0.71 17
rs1333045 0.776 0.280 9 22119196 non coding transcript exon variant T/C snv 0.50 14
rs4841132 8 9326086 non coding transcript exon variant A/G snv 0.89 14
rs7865618 0.776 0.240 9 22031006 non coding transcript exon variant G/A;T snv 11
rs445925 0.882 0.080 19 44912383 non coding transcript exon variant G/A;C snv 10
rs7857345 0.925 0.080 9 22087474 non coding transcript exon variant T/A;C snv 4
rs10738605 0.925 0.120 9 22049131 non coding transcript exon variant C/A;G snv 3
rs1008878 1.000 0.040 9 22036113 non coding transcript exon variant G/T snv 0.71 2
rs10811641 1.000 0.040 9 22014138 non coding transcript exon variant C/G snv 0.32 2
rs1556515 1.000 0.040 9 22036368 non coding transcript exon variant C/T snv 0.71 2