rs104894895

Orientation

minus

Stabilized

minus

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

Make rs104894895(C;G)

Make rs104894895(G;G)

Reference

GRCh38 38.1/141

Chromosome

X

Position

30308551

Gene

NR0B1

is a	snp
is	mentioned by
dbSNP	rs104894895
dbSNP (classic)	rs104894895
ClinGen	rs104894895
ebi	rs104894895
HLI	rs104894895
Exac	rs104894895
Gnomad	rs104894895
Varsome	rs104894895
LitVar	rs104894895
Map	rs104894895
PheGenI	rs104894895
Biobank	rs104894895
1000 genomes	rs104894895
hgdp	rs104894895
ensembl	rs104894895
geneview	rs104894895
scholar	rs104894895
google	rs104894895
pharmgkb	rs104894895
gwascentral	rs104894895
openSNP	rs104894895
23andMe	rs104894895
SNPshot	rs104894895
SNPdbe	rs104894895
MSV3d	rs104894895
GWAS Ctlg	rs104894895

Max Magnitude

0

OMIM	300473
Desc
Variant	0010
Related	also

ClinVar
Risk	rs104894895(G;G)
Alt	rs104894895(G;G)
Reference	Rs104894895(C;C)
Significance	Pathogenic
Disease	Congenital adrenal hypoplasia
Variation	info
Gene	NR0B1
CLNDBN	Congenital adrenal hypoplasia, X-linked
Reversed	1
HGVS	NC_000023.10:g.30326668G>C
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000011706.5,