rs1060499835

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(A;A)	0	common in clinvar

Make rs1060499835(A;C)

Make rs1060499835(C;C)

Reference

GRCh38.p7 38.3/150

Chromosome

X

Position

30308516

Gene

NR0B1

is a	snp
is	mentioned by
dbSNP	rs1060499835
dbSNP (classic)	rs1060499835
ClinGen	rs1060499835
ebi	rs1060499835
HLI	rs1060499835
Exac	rs1060499835
Gnomad	rs1060499835
Varsome	rs1060499835
LitVar	rs1060499835
Map	rs1060499835
PheGenI	rs1060499835
Biobank	rs1060499835
1000 genomes	rs1060499835
hgdp	rs1060499835
ensembl	rs1060499835
geneview	rs1060499835
scholar	rs1060499835
google	rs1060499835
pharmgkb	rs1060499835
gwascentral	rs1060499835
openSNP	rs1060499835
23andMe	rs1060499835
SNPshot	rs1060499835
SNPdbe	rs1060499835
MSV3d	rs1060499835
GWAS Ctlg	rs1060499835

Max Magnitude

0

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,