rs104894898

Orientation

minus

Stabilized

minus

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

Make rs104894898(A;A)

Make rs104894898(A;C)

Reference

GRCh38 38.1/141

Chromosome

X

Position

30308773

Gene

NR0B1

is a	snp
is	mentioned by
dbSNP	rs104894898
dbSNP (classic)	rs104894898
ClinGen	rs104894898
ebi	rs104894898
HLI	rs104894898
Exac	rs104894898
Gnomad	rs104894898
Varsome	rs104894898
LitVar	rs104894898
Map	rs104894898
PheGenI	rs104894898
Biobank	rs104894898
1000 genomes	rs104894898
hgdp	rs104894898
ensembl	rs104894898
geneview	rs104894898
scholar	rs104894898
google	rs104894898
pharmgkb	rs104894898
gwascentral	rs104894898
openSNP	rs104894898
23andMe	rs104894898
SNPshot	rs104894898
SNPdbe	rs104894898
MSV3d	rs104894898
GWAS Ctlg	rs104894898

Max Magnitude

0

OMIM	300473
Desc
Variant	0021
Related	also

ClinVar
Risk	rs104894898(A;A) rs104894898(T;T)
Alt	rs104894898(A;A) rs104894898(T;T)
Reference	Rs104894898(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.30326890G>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000011715.6,