Have questions? Visit https://www.reddit.com/r/SNPedia

rs387907373

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs387907373(G;T)
Make rs387907373(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position30304718
GeneNR0B1
is asnp
is mentioned by
dbSNPrs387907373
ebirs387907373
HLIrs387907373
Exacrs387907373
Varsomers387907373
Maprs387907373
PheGenIrs387907373
hapmaprs387907373
1000 genomesrs387907373
hgdprs387907373
ensemblrs387907373
gopubmedrs387907373
geneviewrs387907373
scholarrs387907373
googlers387907373
pharmgkbrs387907373
gwascentralrs387907373
openSNPrs387907373
23andMers387907373
23andMe allrs387907373
SNP Nexus

SNPshotrs387907373
SNPdbers387907373
MSV3drs387907373
GWAS Ctlgrs387907373
Max Magnitude0
ClinVar
Risk rs387907373(T;T)
Alt rs387907373(T;T)
Reference rs387907373(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.30322835C>A
CLNSRC ClinVar
CLNACC RCV000049288.1,