Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9349205 6 41957421 intron variant G/A;C snv 6
rs112233623 6 41957260 intron variant C/T snv 7.0E-03 5
rs3218097 6 41937537 intron variant G/A;T snv 5
rs9394841 6 41959197 intron variant T/C snv 0.22 3
rs11970772 6 41957552 intron variant T/A snv 0.24 2
rs16895130 6 41957193 intron variant A/G snv 0.22 2
rs9296369 6 41953258 intron variant C/G;T snv 2
rs9369327 6 42046566 intron variant C/T snv 6.5E-02 1
rs9367125 6 42019806 intron variant G/C snv 0.10 1
rs182679717 6 42007955 intron variant C/A;T snv 1