Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs757318 19 18709498 intron variant C/A;G;T snv 3
rs2003476 19 18695858 intron variant T/C snv 0.53 2
rs10221489 19 18716165 intron variant C/T snv 0.38 1
rs11668500 19 18725864 intron variant C/A;G;T snv 1
rs8112818 19 18701975 intron variant A/C;G snv 1