Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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