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rs72552756

From SNPedia

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Stabilizedplus
Geno Mag Summary
(C;C) 5 Congenital adrenal hyperplasia
(C;G) 3 Carrier of allele for congenital adrenal hyperplasia
(G;G) 0 common in complete genomics
ReferenceGRCh38 38.1/141
Chromosome6
Position32040692
GeneCYP21A2, TNXB
is asnp
is mentioned by
dbSNPrs72552756
dbSNP (classic)rs72552756
ClinGenrs72552756
ebirs72552756
HLIrs72552756
Exacrs72552756
Gnomadrs72552756
Varsomers72552756
LitVarrs72552756
Maprs72552756
PheGenIrs72552756
Biobankrs72552756
1000 genomesrs72552756
hgdprs72552756
ensemblrs72552756
geneviewrs72552756
scholarrs72552756
googlers72552756
pharmgkbrs72552756
gwascentralrs72552756
openSNPrs72552756
23andMers72552756
SNPshotrs72552756
SNPdbers72552756
MSV3drs72552756
GWAS Ctlgrs72552756
Max Magnitude5
OMIM201910
Desc
Variant0023
Relatedalso
ClinVar
Risk Rs72552756(C;C)
Alt Rs72552756(C;C)
Reference Rs72552756(G;G)
Significance Untested
Disease
Variation info
Gene TNXB CYP21A2
CLNDBN
Reversed 0
HGVS NC_000006.11:g.32008469G>C
CLNSRC
CLNACC