rs104894906

Orientation

minus

Stabilized

minus

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

Make rs104894906(A;A)

Make rs104894906(A;C)

Reference

GRCh38 38.1/141

Chromosome

X

Position

30304795

Gene

NR0B1

is a	snp
is	mentioned by
dbSNP	rs104894906
dbSNP (classic)	rs104894906
ClinGen	rs104894906
ebi	rs104894906
HLI	rs104894906
Exac	rs104894906
Gnomad	rs104894906
Varsome	rs104894906
LitVar	rs104894906
Map	rs104894906
PheGenI	rs104894906
Biobank	rs104894906
1000 genomes	rs104894906
hgdp	rs104894906
ensembl	rs104894906
geneview	rs104894906
scholar	rs104894906
google	rs104894906
pharmgkb	rs104894906
gwascentral	rs104894906
openSNP	rs104894906
23andMe	rs104894906
SNPshot	rs104894906
SNPdbe	rs104894906
MSV3d	rs104894906
GWAS Ctlg	rs104894906

Max Magnitude

0

OMIM	300473
Desc
Variant	0027
Related	also

ClinVar
Risk	rs104894906(A;A)
Alt	rs104894906(A;A)
Reference	Rs104894906(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.30322912G>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000011722.10,