Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10507391 0.776 0.320 13 30737959 intron variant A/T snv 0.52 10
rs9551963 0.851 0.160 13 30758410 intron variant A/C;T snv 6
rs9579646 0.851 0.160 13 30736442 intron variant G/A;T snv 6
rs12429692 1.000 0.080 13 30738041 intron variant A/T snv 0.24 2
rs17222919 1.000 0.080 13 30734192 intron variant T/A;G snv 2
rs3803277 13 30744171 non coding transcript exon variant C/A snv 0.49 0.45 1
rs4769060 13 30763740 intron variant A/G snv 0.35 1