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rs267606755

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs267606755(G;G)
Make rs267606755(G;T)
ReferenceGRCh38 38.1/141
Chromosome8
Position142875086
GeneCYP11B1
is asnp
is mentioned by
dbSNPrs267606755
ebirs267606755
HLIrs267606755
Exacrs267606755
Varsomers267606755
Maprs267606755
PheGenIrs267606755
hapmaprs267606755
1000 genomesrs267606755
hgdprs267606755
ensemblrs267606755
gopubmedrs267606755
geneviewrs267606755
scholarrs267606755
googlers267606755
pharmgkbrs267606755
gwascentralrs267606755
openSNPrs267606755
23andMers267606755
23andMe allrs267606755
SNP Nexus

SNPshotrs267606755
SNPdbers267606755
MSV3drs267606755
GWAS Ctlgrs267606755
Max Magnitude0
ClinVar
Risk rs267606755(G;G)
Alt rs267606755(G;G)
Reference rs267606755(T;T)
Significance Pathogenic
Disease Deficiency of steroid 11-beta-monooxygenase
Variation info
Gene CYP11B1
CLNDBN Deficiency of steroid 11-beta-monooxygenase
Reversed 1
HGVS NC_000008.10:g.143956502A>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000001244.2,