Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1372519 1.000 0.040 4 89836158 5 prime UTR variant A/G snv 0.77 1
rs2583988 0.925 0.080 4 89839677 non coding transcript exon variant C/A;T snv 1
rs11931074 0.851 0.080 4 89718364 intron variant G/A;C;T snv 1
rs2572323 1.000 0.040 4 89713401 intron variant A/G snv 0.75 1
rs356174 1.000 0.040 4 89709750 intron variant G/T snv 0.72 1
rs356180 1.000 0.040 4 89706976 intron variant A/G snv 0.77 1
rs1372520 1.000 0.040 4 89836354 intron variant T/C snv 0.78 1