Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs13240401 7 2154761 intron variant T/A;C snv 1
rs34782622 7 2155497 intron variant A/G snv 0.14 1
rs62442924 7 1950341 intron variant C/T snv 0.17 1
rs71525361 7 2120142 intron variant T/A;C snv 1
rs11772232 7 1816637 intron variant C/T snv 0.13 1