Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1122608 0.763 0.120 19 11052925 intron variant G/T snv 0.18 3
rs112374545 19 11078223 intron variant C/T snv 0.11 2
rs12052201 19 11048420 intron variant G/T snv 0.17 2
rs143020224 19 11076648 intron variant C/G;T snv 2
rs17001095 19 11022596 intron variant A/G snv 0.33 2
rs3786722 19 11050861 intron variant C/A snv 0.18 2
rs73015011 19 11079088 missense variant T/C snv 0.13 2
rs11669133 1.000 0.040 19 10981463 intron variant G/A snv 4.2E-02 1