Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10411210 0.742 0.160 19 33041394 intron variant C/T snv 0.22 13
rs28840750 0.776 0.080 19 33029021 intron variant T/G snv 7.6E-02 10
rs13343954 0.790 0.080 19 33036982 intron variant T/C snv 0.18 9
rs73039434 0.790 0.080 19 33034013 intron variant T/G snv 0.13 9