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Rs104894899

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Orientationminus
is asnp
is mentioned by
dbSNPrs104894899
PheGenIrs104894899
nextbiors104894899
hapmaprs104894899
1000 genomesrs104894899
hgdprs104894899
ensemblrs104894899
gopubmedrs104894899
geneviewrs104894899
scholarrs104894899
googlers104894899
pharmgkbrs104894899
gwascentralrs104894899
openSNPrs104894899
23andMers104894899
23andMe allrs104894899
SNP Nexus

SNPshotrs104894899
SNPdbers104894899
MSV3drs104894899
GeneNR0B1
ChromosomeX
Orientationminus
Position30308222
ReferenceGRCh38 38.1/141
Max Magnitude0
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs104894899(A;A)
Make rs104894899(A;T)
OMIM300473
Desc
Variant0023
Relatedalso
ClinVar
Risk rs104894899(A;A)
Alt rs104894899(A;A)
Reference rs104894899(T;T)
Significance 5
Disease Congenital adrenal hypoplasia
ClinVar info
Gene NR0B1
CLNDBN Congenital adrenal hypoplasia, X-linked
Reversed 1
CLNHGVS NC_000023.10:g.30326339A>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000011718.5