Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7169629 15 84648043 non coding transcript exon variant C/G snv 0.51 1
rs35258188 1.000 0.040 15 53705141 missense variant T/G snv 3.5E-03 1.5E-02 4
rs17730281 1.000 0.080 15 53615751 missense variant G/A snv 0.26 0.22 3
rs1906436 1.000 0.040 15 53590245 intron variant T/C snv 0.32 3
rs491567 1.000 0.080 15 53654396 intron variant A/C snv 0.34 3
rs10518732 15 53646845 intron variant G/A;C snv 2
rs1031755 15 53659238 intron variant A/C snv 0.22 1
rs10851543 15 53670551 intron variant A/G snv 0.32 1
rs35255404 15 53627029 intron variant G/A snv 0.21 1
rs5812700 15 53629192 intron variant AGAGAG/-;AG;AGAG;AGAGAGAG;AGAGAGAGAG;AGAGAGAGAGAG;AGAGAGAGAGAGAG delins 1
rs62005941 15 53623569 intron variant C/A;G snv 1
rs690428 15 53658381 intron variant A/C snv 0.35 1
rs7169329 15 53610429 intron variant C/G snv 0.62 1
rs10794720 1.000 0.080 10 1110225 intron variant T/C snv 0.89 3
rs3775932 4 10089306 intron variant C/A snv 0.47 1
rs538063388 22 42049977 intron variant AAAAAAAAAAAAAAA/-;A;AA;AAA;AAAAAA;AAAAAAA;AAAAAAAA;AAAAAAAAA;AAAAAAAAAA;AAAAAAAAAAA;AAAAAAAAAAAA;AAAAAAAAAAAAA;AAAAAAAAAAAAAA;AAAAAAAAAAAAAAAA;AAAAAAAAAAAAAAAAA;AAAAAAAAAAAAAAAAAA;AAAAAAAAAAAAAAAAAAA;AAAAAAAAAAAAAAAAAAAA delins 9.2E-02 1
rs284859 10 102813260 missense variant G/A;T snv 8.1E-06; 0.20 1
rs6892 10 102816113 3 prime UTR variant A/G snv 0.15 1
rs55773927 7 65872915 upstream gene variant T/C;G snv 1
rs17462630 2 218421818 intron variant G/A;C snv 0.24 1
rs138551969 1.000 0.040 6 43780749 missense variant A/G snv 1.2E-05 3.5E-05 4
rs11100781 4 143211469 intron variant A/G;T snv 1
rs988911 2 61380375 intron variant G/A;T snv 0.19; 4.3E-06 1
rs6589750 11 119456016 intron variant G/A snv 0.58 1
rs17818393 2 209989752 intron variant A/G snv 0.51 1