Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1812175 4 144653692 intron variant A/G snv 0.79 5
rs2131354 4 144678756 intron variant G/A snv 0.41 2
rs7689420 0.851 0.080 4 144647200 non coding transcript exon variant T/C snv 0.79 2
rs6845999 4 144644674 intron variant C/T snv 0.35 2
rs1492820 4 144728869 intron variant G/A snv 0.50 1
rs6854783 4 144721927 intron variant G/A;C snv 1
rs13106087 4 144645712 non coding transcript exon variant T/C;G snv 1
rs13125694 4 144645696 intron variant C/T snv 0.34 1