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: rs72552751
rs72552751
CYP21A2
2 0.925 0.200 6 32039444 missense variant G/C snv 0.010 1.000 1 1999 1999
dbSNP: rs760216630
rs760216630
CYP21A2
2 0.925 0.200 6 32040530 missense variant G/A snv 0.010 1.000 1 1999 1999