Rs104894889

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Orientationminus
is asnp
is mentioned by
dbSNPrs104894889
PheGenIrs104894889
nextbiors104894889
hapmaprs104894889
1000 genomesrs104894889
hgdprs104894889
ensemblrs104894889
gopubmedrs104894889
geneviewrs104894889
scholarrs104894889
googlers104894889
pharmgkbrs104894889
gwascentralrs104894889
openSNPrs104894889
23andMers104894889
23andMe allrs104894889
SNP Nexus

SNPshotrs104894889
SNPdbers104894889
MSV3drs104894889
GeneNR0B1
ChromosomeX
Orientationminus
Position30308660
ReferenceGRCh38 38.1/141
Max Magnitude0
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs104894889(A;A)
Make rs104894889(A;G)
OMIM300473
Desc
Variant0005
Relatedalso
ClinVar
Risk rs104894889(A;A)
Alt rs104894889(A;A)
Reference rs104894889(G;G)
Significance 5
Disease Congenital adrenal hypoplasia
ClinVar info
Gene NR0B1
CLNDBN Congenital adrenal hypoplasia, X-linked
Reversed 1
CLNHGVS NC_000023.10:g.30326777C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000011700.1