Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11220463 11 126378316 intron variant A/T snv 0.12 3
rs68055275 11 126369248 intron variant -/T;TT delins 3
rs76970536 11 126380785 intron variant G/A;T snv 3
rs10893499 11 126372084 intron variant G/A snv 0.16 2
rs11220462 11 126374057 intron variant G/A snv 0.12 2
rs4307732 11 126375060 non coding transcript exon variant G/A snv 0.13 2
rs59379014 11 126358105 intron variant C/T snv 0.12 2