Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10832134 1.000 0.040 11 2481256 intron variant C/A;T snv 1
rs11523905 1.000 0.040 11 2477029 intron variant G/A;C;T snv 1
rs12576156 1.000 0.040 11 2477588 intron variant A/G snv 0.22 1