Rs104894891

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Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs104894891(A;A)
Make rs104894891(A;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position30308851
GeneNR0B1
is asnp
is mentioned by
dbSNPrs104894891
PheGenIrs104894891
nextbiors104894891
hapmaprs104894891
1000 genomesrs104894891
hgdprs104894891
ensemblrs104894891
gopubmedrs104894891
geneviewrs104894891
scholarrs104894891
googlers104894891
pharmgkbrs104894891
gwascentralrs104894891
openSNPrs104894891
23andMers104894891
23andMe allrs104894891
SNP Nexus

SNPshotrs104894891
SNPdbers104894891
MSV3drs104894891
Max Magnitude0
OMIM300473
Desc
Variant0006
Relatedalso
ClinVar
Risk rs104894891(A;A)
Alt rs104894891(A;A)
Reference rs104894891(G;G)
Significance Pathogenic
Disease Congenital adrenal hypoplasia
Variation info
Gene NR0B1
CLNDBN Congenital adrenal hypoplasia, X-linked
Reversed 1
HGVS NC_000023.10:g.30326968C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000011701.5,