Rs104894890

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Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs104894890(C;T)
Make rs104894890(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position30308517
GeneNR0B1
is asnp
is mentioned by
dbSNPrs104894890
PheGenIrs104894890
nextbiors104894890
hapmaprs104894890
1000 genomesrs104894890
hgdprs104894890
ensemblrs104894890
gopubmedrs104894890
geneviewrs104894890
scholarrs104894890
googlers104894890
pharmgkbrs104894890
gwascentralrs104894890
openSNPrs104894890
23andMers104894890
23andMe allrs104894890
SNP Nexus

SNPshotrs104894890
SNPdbers104894890
MSV3drs104894890
Max Magnitude0
OMIM300473
Desc
Variant0001
Relatedalso
ClinVar
Risk rs104894890(T;T)
Alt rs104894890(T;T)
Reference rs104894890(C;C)
Significance Pathogenic
Disease Congenital adrenal hypoplasia
Variation info
Gene NR0B1
CLNDBN Congenital adrenal hypoplasia, X-linked
Reversed 1
HGVS NC_000023.10:g.30326634G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000011696.4,