Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs17032907
CA6
0.925 0.040 1 8950346 intron variant C/T snv 0.17 2
rs2274328
CA6
0.925 0.040 1 8949385 missense variant A/C snv 0.49 0.51 2
rs11576766
CA6
1.000 1 8950925 intron variant A/C;T snv 1