Source: ALL
Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs11576766
rs11576766
CA6
1 1.000 1 8950925 intron variant A/C;T snv 0.010 < 0.001 1 2015 2015
dbSNP: rs17032907
rs17032907
CA6
2 0.925 0.040 1 8950346 intron variant C/T snv 0.17 0.010 < 0.001 1 2015 2015
dbSNP: rs2274328
rs2274328
CA6
2 0.925 0.040 1 8949385 missense variant A/C snv 0.49 0.51 0.010 < 0.001 1 2015 2015