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: rs1560567337
rs1560567337
PPP3CA
1 1.000 4 101026014 missense variant C/T snv 0.700 0
dbSNP: rs1560567347
rs1560567347
PPP3CA
1 1.000 4 101026023 missense variant A/G snv 0.700 0