Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10127775 1 230160042 intron variant A/G;T snv 4
rs10864728 1 230169168 intron variant A/G snv 0.50 3
rs10489615 1 230169242 intron variant A/C;G snv 2
rs1321257 1 230169566 intron variant G/A snv 0.50 2
rs2144300 0.882 0.040 1 230159169 intron variant C/T snv 0.44 2
rs4846914 0.925 0.080 1 230159944 intron variant G/A snv 0.45 2
rs4846923 1 230171476 intron variant T/G snv 0.72 2
rs17315646 1 230159560 intron variant C/A;G snv 0.45 1
rs2281719 1.000 0.040 1 230161913 intron variant C/T snv 0.45 1