Rs104894897

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Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs104894897(G;G)
Make rs104894897(G;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position30304676
GeneNR0B1
is asnp
is mentioned by
dbSNPrs104894897
Exacrs104894897
PheGenIrs104894897
nextbiors104894897
hapmaprs104894897
1000 genomesrs104894897
hgdprs104894897
ensemblrs104894897
gopubmedrs104894897
geneviewrs104894897
scholarrs104894897
googlers104894897
pharmgkbrs104894897
gwascentralrs104894897
openSNPrs104894897
23andMers104894897
23andMe allrs104894897
SNP Nexus

SNPshotrs104894897
SNPdbers104894897
MSV3drs104894897
Max Magnitude0
OMIM300473
Desc
Variant0020
Relatedalso
ClinVar
Risk rs104894897(G;G)
Alt rs104894897(G;G)
Reference rs104894897(T;T)
Significance Pathogenic
Disease Congenital adrenal hypoplasia
Variation info
Gene NR0B1
CLNDBN Congenital adrenal hypoplasia, X-linked
Reversed 1
HGVS NC_000023.10:g.30322793A>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000011716.1,