Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7852169 9 111556114 intron variant C/G snv 0.15 2
rs10980926 9 111531354 intron variant A/G snv 0.56 2
rs10217747 9 111547655 3 prime UTR variant T/A;C snv 1
rs10441737 9 111539305 intron variant C/T snv 0.59 1
rs7873730 9 111541399 intron variant A/T snv 0.11 1