rs104894886

Orientation

minus

Stabilized

minus

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

Make rs104894886(A;A)

Make rs104894886(A;G)

Reference

GRCh38 38.1/141

Chromosome

X

Position

30308257

Gene

NR0B1

is a	snp
is	mentioned by
dbSNP	rs104894886
dbSNP (classic)	rs104894886
ClinGen	rs104894886
ebi	rs104894886
HLI	rs104894886
Exac	rs104894886
Gnomad	rs104894886
Varsome	rs104894886
LitVar	rs104894886
Map	rs104894886
PheGenI	rs104894886
Biobank	rs104894886
1000 genomes	rs104894886
hgdp	rs104894886
ensembl	rs104894886
geneview	rs104894886
scholar	rs104894886
google	rs104894886
pharmgkb	rs104894886
gwascentral	rs104894886
openSNP	rs104894886
23andMe	rs104894886
SNPshot	rs104894886
SNPdbe	rs104894886
MSV3d	rs104894886
GWAS Ctlg	rs104894886

Max Magnitude

0

OMIM	300473
Desc
Variant	0002
Related	also

ClinVar
Risk	rs104894886(A;A)
Alt	rs104894886(A;A)
Reference	Rs104894886(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.30326374C>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000011697.9,