rs104894900

Orientation

minus

Stabilized

minus

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

Make rs104894900(G;G)

Make rs104894900(G;T)

Reference

GRCh38 38.1/141

Chromosome

X

Position

30308226

Gene

NR0B1

is a	snp
is	mentioned by
dbSNP	rs104894900
dbSNP (classic)	rs104894900
ClinGen	rs104894900
ebi	rs104894900
HLI	rs104894900
Exac	rs104894900
Gnomad	rs104894900
Varsome	rs104894900
LitVar	rs104894900
Map	rs104894900
PheGenI	rs104894900
Biobank	rs104894900
1000 genomes	rs104894900
hgdp	rs104894900
ensembl	rs104894900
geneview	rs104894900
scholar	rs104894900
google	rs104894900
pharmgkb	rs104894900
gwascentral	rs104894900
openSNP	rs104894900
23andMe	rs104894900
SNPshot	rs104894900
SNPdbe	rs104894900
MSV3d	rs104894900
GWAS Ctlg	rs104894900

Max Magnitude

0

OMIM	300473
Desc
Variant	0025
Related	also

ClinVar
Risk	rs104894900(G;G)
Alt	rs104894900(G;G)
Reference	Rs104894900(T;T)
Significance	Pathogenic
Disease	Congenital adrenal hypoplasia
Variation	info
Gene	NR0B1
CLNDBN	Congenital adrenal hypoplasia, X-linked
Reversed	1
HGVS	NC_000023.10:g.30326343A>C
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000011720.2,