rs104894893

Orientation

minus

Stabilized

minus

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

Make rs104894893(A;A)

Make rs104894893(A;G)

Reference

GRCh38 38.1/141

Chromosome

X

Position

30308852

Gene

NR0B1

is a	snp
is	mentioned by
dbSNP	rs104894893
dbSNP (classic)	rs104894893
ClinGen	rs104894893
ebi	rs104894893
HLI	rs104894893
Exac	rs104894893
Gnomad	rs104894893
Varsome	rs104894893
LitVar	rs104894893
Map	rs104894893
PheGenI	rs104894893
Biobank	rs104894893
1000 genomes	rs104894893
hgdp	rs104894893
ensembl	rs104894893
geneview	rs104894893
scholar	rs104894893
google	rs104894893
pharmgkb	rs104894893
gwascentral	rs104894893
openSNP	rs104894893
23andMe	rs104894893
SNPshot	rs104894893
SNPdbe	rs104894893
MSV3d	rs104894893
GWAS Ctlg	rs104894893

Max Magnitude

0

OMIM	300473
Desc
Variant	0006
Related	also

ClinVar
Risk	rs104894893(A;A)
Alt	rs104894893(A;A)
Reference	Rs104894893(G;G)
Significance	Untested
Disease	Congenital adrenal hypoplasia
Variation	info
Gene	NR0B1
CLNDBN	Congenital adrenal hypoplasia, X-linked
Reversed	1
HGVS	NC_000023.10:g.30326969C>T
CLNSRC	OMIM Allelic Variant
CLNACC	SCV000031933.1, SCV000031933.1,