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: rs104893978
rs104893978
CYP21A2 ; NEU1
2 0.925 0.160 6 31860519 missense variant A/G snv 1.4E-05 0.010 1.000 1 2002 2002
dbSNP: rs104893985
rs104893985
CYP21A2 ; NEU1
2 0.925 0.160 6 31862112 missense variant G/A snv 2.4E-05 7.0E-06 0.010 1.000 1 2002 2002