rs104894894

Orientation

minus

Stabilized

minus

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

Make rs104894894(C;T)

Make rs104894894(T;T)

Reference

GRCh38 38.1/141

Chromosome

X

Position

30304809

Gene

NR0B1

is a	snp
is	mentioned by
dbSNP	rs104894894
dbSNP (classic)	rs104894894
ClinGen	rs104894894
ebi	rs104894894
HLI	rs104894894
Exac	rs104894894
Gnomad	rs104894894
Varsome	rs104894894
LitVar	rs104894894
Map	rs104894894
PheGenI	rs104894894
Biobank	rs104894894
1000 genomes	rs104894894
hgdp	rs104894894
ensembl	rs104894894
geneview	rs104894894
scholar	rs104894894
google	rs104894894
pharmgkb	rs104894894
gwascentral	rs104894894
openSNP	rs104894894
23andMe	rs104894894
SNPshot	rs104894894
SNPdbe	rs104894894
MSV3d	rs104894894
GWAS Ctlg	rs104894894

Max Magnitude

0

OMIM	300473
Desc
Variant	0009
Related	also

ClinVar
Risk	rs104894894(T;T)
Alt	rs104894894(T;T)
Reference	Rs104894894(C;C)
Significance	Pathogenic
Disease	Congenital adrenal hypoplasia not provided
Variation	info
Gene	NR0B1
CLNDBN	Congenital adrenal hypoplasia, X-linked not provided
Reversed	1
HGVS	NC_000023.10:g.30322926G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000011705.9, RCV000481802.1,