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rs397515532

From SNPedia

Merged intors267606756
Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs397515532(-;T)
Make rs397515532(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position32040189
GeneCYP21A2
is asnp
is mentioned by
dbSNPrs397515532
dbSNP (old)rs397515532
ClinGenrs397515532
ebirs397515532
HLIrs397515532
Exacrs397515532
Varsomers397515532
Maprs397515532
PheGenIrs397515532
Biobankrs397515532
1000 genomesrs397515532
hgdprs397515532
ensemblrs397515532
gopubmedrs397515532
geneviewrs397515532
scholarrs397515532
googlers397515532
pharmgkbrs397515532
gwascentralrs397515532
openSNPrs397515532
23andMers397515532
23andMe allrs397515532
SNP Nexus

SNPshotrs397515532
SNPdbers397515532
MSV3drs397515532
GWAS Ctlgrs397515532
StatusMerged into rs267606756
Max Magnitude0
ClinVar
Risk rs397515532(T;T)
Alt rs397515532(T;T)
Reference Rs397515532(;)
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,