Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs201272561
AUH
9 91334470 intron variant C/T snv 4.2E-05 2
rs7020893
AUH
9 91359048 intron variant G/A snv 0.21 1
rs56049491
AUH
9 91218276 intron variant T/A snv 0.12 1