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rs28935481

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
(T;T) 0
Make rs28935481(A;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position30304673
GeneNR0B1
is asnp
is mentioned by
dbSNPrs28935481
ebirs28935481
HLIrs28935481
Exacrs28935481
Varsomers28935481
Maprs28935481
PheGenIrs28935481
hapmaprs28935481
1000 genomesrs28935481
hgdprs28935481
ensemblrs28935481
gopubmedrs28935481
geneviewrs28935481
scholarrs28935481
googlers28935481
pharmgkbrs28935481
gwascentralrs28935481
openSNPrs28935481
23andMers28935481
23andMe allrs28935481
SNP Nexus

SNPshotrs28935481
SNPdbers28935481
MSV3drs28935481
GWAS Ctlgrs28935481
Max Magnitude0
OMIM300473
DescADRENAL HYPOPLASIA, CONGENITAL
Variant0008
Relatedalso
Neighborrs28935482
Distance3818


ClinVar
Risk rs28935481(T;T)
Alt rs28935481(T;T)
Reference rs28935481(A;A)
Significance Pathogenic
Disease Congenital adrenal hypoplasia
Variation info
Gene NR0B1
CLNDBN Congenital adrenal hypoplasia, X-linked
Reversed 1
HGVS NC_000023.10:g.30322790T>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000011704.3,