rs72554626, CYP11B2;GML

N. diseases: 1
Source: UNIPROT ×
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Corticosterone Methyl Oxidase Type II Deficiency
CUI: C3463917
Disease: Corticosterone Methyl Oxidase Type II Deficiency
5 1.000 8 142912000 missense variant T/C snv 0.800 1.000 5 1992 2003