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: rs1532423
rs1532423
CA1
2 8 85356084 intron variant A/G;T snv 0.700 1.000 1 2016 2016
dbSNP: rs6997458
rs6997458
CA1
1 8 85361801 intron variant T/A;G snv 0.700 1.000 1 2016 2016