rs104894907

Orientation

minus

Stabilized

minus

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

Make rs104894907(C;C)

Make rs104894907(C;T)

Reference

GRCh38 38.1/141

Chromosome

X

Position

30308474

Gene

NR0B1

is a	snp
is	mentioned by
dbSNP	rs104894907
dbSNP (classic)	rs104894907
ClinGen	rs104894907
ebi	rs104894907
HLI	rs104894907
Exac	rs104894907
Gnomad	rs104894907
Varsome	rs104894907
LitVar	rs104894907
Map	rs104894907
PheGenI	rs104894907
Biobank	rs104894907
1000 genomes	rs104894907
hgdp	rs104894907
ensembl	rs104894907
geneview	rs104894907
scholar	rs104894907
google	rs104894907
pharmgkb	rs104894907
gwascentral	rs104894907
openSNP	rs104894907
23andMe	rs104894907
SNPshot	rs104894907
SNPdbe	rs104894907
MSV3d	rs104894907
GWAS Ctlg	rs104894907

Max Magnitude

0

OMIM	300473
Desc
Variant	0028
Related	also

ClinVar
Risk	rs104894907(C;C)
Alt	rs104894907(C;C)
Reference	Rs104894907(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.30326591A>G
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000011723.7,