Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs746540053 1.000 0.040 1 207911034 missense variant C/T snv 2
rs2724379 1.000 0.080 1 207903511 intron variant A/C snv 0.24 1
rs6671850 1 207884455 3 prime UTR variant C/T snv 8.7E-02 1