Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4871752 8 126908341 intron variant G/A snv 0.43 1
rs7817717 8 126891017 intron variant T/G snv 0.43 1
rs4871750 8 126889758 intron variant G/A;C snv 1
rs7012789 8 126904963 intron variant A/G;T snv 1