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rs267606756

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs267606756(-;-)
Make rs267606756(-;T)
Make rs267606756(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position32040186
GeneCYP21A2
is asnp
is mentioned by
dbSNPrs267606756
ebirs267606756
HLIrs267606756
Exacrs267606756
Varsomers267606756
Maprs267606756
PheGenIrs267606756
hapmaprs267606756
1000 genomesrs267606756
hgdprs267606756
ensemblrs267606756
gopubmedrs267606756
geneviewrs267606756
scholarrs267606756
googlers267606756
pharmgkbrs267606756
gwascentralrs267606756
openSNPrs267606756
23andMers267606756
23andMe allrs267606756
SNP Nexus

SNPshotrs267606756
SNPdbers267606756
MSV3drs267606756
GWAS Ctlgrs267606756
Max Magnitude0
ClinVar
Risk rs267606756(T;T)
Alt rs267606756(T;T)
Reference rs267606756(;)
Significance Pathogenic
Disease 21-hydroxylase deficiency
Variation info
Gene CYP21A2
CLNDBN 21-hydroxylase deficiency
Reversed 0
HGVS NC_000006.11:g.32007966dupT
CLNSRC OMIM Allelic Variant
CLNACC RCV000055821.3,