rs72558405

Orientation

plus

Stabilized

plus

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

Make rs72558405(A;G)

Make rs72558405(G;G)

Reference

GRCh38 38.1/141

Chromosome

X

Position

38403672

Gene

OTC

is a	snp
is	mentioned by
dbSNP	rs72558405
dbSNP (classic)	rs72558405
ClinGen	rs72558405
ebi	rs72558405
HLI	rs72558405
Exac	rs72558405
Gnomad	rs72558405
Varsome	rs72558405
LitVar	rs72558405
Map	rs72558405
PheGenI	rs72558405
Biobank	rs72558405
1000 genomes	rs72558405
hgdp	rs72558405
ensembl	rs72558405
geneview	rs72558405
scholar	rs72558405
google	rs72558405
pharmgkb	rs72558405
gwascentral	rs72558405
openSNP	rs72558405
23andMe	rs72558405
SNPshot	rs72558405
SNPdbe	rs72558405
MSV3d	rs72558405
GWAS Ctlg	rs72558405

Max Magnitude

0

ClinVar
Risk	rs72558405(G;G)
Alt	rs72558405(G;G)
Reference	Rs72558405(A;A)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	OTC
CLNDBN	not provided
Reversed	0
HGVS	NC_000023.10:g.38262925A>G
CLNSRC	ClinVar
CLNACC	RCV000083506.1,