Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1017281 1.000 0.040 8 130234967 intron variant G/A snv 0.37 1
rs10956514 1.000 0.040 8 130240512 intron variant A/G snv 0.37 1
rs11774633 1.000 0.040 8 130177997 intron variant C/T snv 0.61 1
rs4236749 1.000 0.040 8 130052907 3 prime UTR variant C/T snv 0.16 1
rs4733781 1.000 0.040 8 130284521 intron variant A/C snv 0.29 1