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

rs1060499835

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1060499835(A;C)
Make rs1060499835(C;C)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position30308516
GeneNR0B1
is asnp
is mentioned by
dbSNPrs1060499835
dbSNP (classic)rs1060499835
ClinGenrs1060499835
ebirs1060499835
HLIrs1060499835
Exacrs1060499835
Gnomadrs1060499835
Varsomers1060499835
LitVarrs1060499835
Maprs1060499835
PheGenIrs1060499835
Biobankrs1060499835
1000 genomesrs1060499835
hgdprs1060499835
ensemblrs1060499835
geneviewrs1060499835
scholarrs1060499835
googlers1060499835
pharmgkbrs1060499835
gwascentralrs1060499835
openSNPrs1060499835
23andMers1060499835
23andMe allrs1060499835
SNPshotrs1060499835
SNPdbers1060499835
MSV3drs1060499835
GWAS Ctlgrs1060499835
Max Magnitude0
ClinVar
Risk rs1060499835(C;C)
Alt rs1060499835(C;C)
Reference Rs1060499835(A;A)
Significance Probable-Pathogenic
Disease Congenital adrenal hypoplasia
Variation info
Gene NR0B1
CLNDBN Congenital adrenal hypoplasia, X-linked
Reversed 1
HGVS NC_000023.10:g.30326633T>G
CLNSRC
CLNACC RCV000462560.1,