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rs72552757

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
(C;T) 3 Carrier of allele for congenital adrenal hyperplasia
(T;T) 5 Congenital adrenal hyperplasia
ReferenceGRCh38 38.1/141
Chromosome6
Position32040871
GeneCYP21A2, TNXB
is asnp
is mentioned by
dbSNPrs72552757
ebirs72552757
HLIrs72552757
Exacrs72552757
Varsomers72552757
Maprs72552757
PheGenIrs72552757
hapmaprs72552757
1000 genomesrs72552757
hgdprs72552757
ensemblrs72552757
gopubmedrs72552757
geneviewrs72552757
scholarrs72552757
googlers72552757
pharmgkbrs72552757
gwascentralrs72552757
openSNPrs72552757
23andMers72552757
23andMe allrs72552757
SNP Nexus

SNPshotrs72552757
SNPdbers72552757
MSV3drs72552757
GWAS Ctlgrs72552757
Max Magnitude5
OMIM201910
Desc
Variant0030
Relatedalso
ClinVar
Risk rs72552757(T;T)
Alt rs72552757(T;T)
Reference rs72552757(C;C)
Significance Untested
Disease
Variation info
Gene TNXB CYP21A2
CLNDBN
Reversed 0
HGVS NC_000006.11:g.32008648C>T
CLNSRC
CLNACC