Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11209718 1 41223266 intron variant C/G;T snv 2
rs6686842 1 41065199 intron variant T/C snv 0.65 2
rs114233776 1 41152625 missense variant G/A snv 4.7E-03 4.7E-03 1
rs6600365 1 41090581 intron variant C/T snv 0.65 1