rs387907373

Orientation

minus

Stabilized

minus

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

Make rs387907373(G;T)

Make rs387907373(T;T)

Reference

GRCh38 38.1/141

Chromosome

X

Position

30304718

Gene

NR0B1

is a	snp
is	mentioned by
dbSNP	rs387907373
dbSNP (classic)	rs387907373
ClinGen	rs387907373
ebi	rs387907373
HLI	rs387907373
Exac	rs387907373
Gnomad	rs387907373
Varsome	rs387907373
LitVar	rs387907373
Map	rs387907373
PheGenI	rs387907373
Biobank	rs387907373
1000 genomes	rs387907373
hgdp	rs387907373
ensembl	rs387907373
geneview	rs387907373
scholar	rs387907373
google	rs387907373
pharmgkb	rs387907373
gwascentral	rs387907373
openSNP	rs387907373
23andMe	rs387907373
SNPshot	rs387907373
SNPdbe	rs387907373
MSV3d	rs387907373
GWAS Ctlg	rs387907373

Max Magnitude

0

ClinVar
Risk	rs387907373(T;T)
Alt	rs387907373(T;T)
Reference	Rs387907373(G;G)
Significance	Pathogenic
Disease	Congenital adrenal hypoplasia
Variation	info
Gene	NR0B1
CLNDBN	Congenital adrenal hypoplasia, X-linked
Reversed	1
HGVS	NC_000023.10:g.30322835C>A
CLNSRC	ClinVar
CLNACC	RCV000049288.1,