Rs104894893

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Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs104894893(A;A)
Make rs104894893(A;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position30308852
GeneNR0B1
is asnp
is mentioned by
dbSNPrs104894893
Exacrs104894893
PheGenIrs104894893
nextbiors104894893
hapmaprs104894893
1000 genomesrs104894893
hgdprs104894893
ensemblrs104894893
gopubmedrs104894893
geneviewrs104894893
scholarrs104894893
googlers104894893
pharmgkbrs104894893
gwascentralrs104894893
openSNPrs104894893
23andMers104894893
23andMe allrs104894893
SNP Nexus

SNPshotrs104894893
SNPdbers104894893
MSV3drs104894893
Max Magnitude0
OMIM300473
Desc
Variant0006
Relatedalso
ClinVar
Risk rs104894893(A;A)
Alt rs104894893(A;A)
Reference rs104894893(G;G)
Significance Untested
Disease Congenital adrenal hypoplasia
Variation info
Gene NR0B1
CLNDBN Congenital adrenal hypoplasia, X-linked
Reversed 1
HGVS NC_000023.10:g.30326969C>T
CLNSRC OMIM Allelic Variant
CLNACC SCV000031933.1, SCV000031933.1,