rs72556263

Orientation

plus

Stabilized

plus

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

Make rs72556263(C;G)

Make rs72556263(G;G)

Reference

GRCh38 38.1/141

Chromosome

X

Position

38401325

Gene

OTC

is a	snp
is	mentioned by
dbSNP	rs72556263
dbSNP (classic)	rs72556263
ClinGen	rs72556263
ebi	rs72556263
HLI	rs72556263
Exac	rs72556263
Gnomad	rs72556263
Varsome	rs72556263
LitVar	rs72556263
Map	rs72556263
PheGenI	rs72556263
Biobank	rs72556263
1000 genomes	rs72556263
hgdp	rs72556263
ensembl	rs72556263
geneview	rs72556263
scholar	rs72556263
google	rs72556263
pharmgkb	rs72556263
gwascentral	rs72556263
openSNP	rs72556263
23andMe	rs72556263
SNPshot	rs72556263
SNPdbe	rs72556263
MSV3d	rs72556263
GWAS Ctlg	rs72556263

Max Magnitude

0

ClinVar
Risk	rs72556263(G;G)
Alt	rs72556263(G;G)
Reference	Rs72556263(C;C)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	OTC
CLNDBN	not provided
Reversed	0
HGVS	NC_000023.10:g.38260578C>G
CLNSRC	ClinVar
CLNACC	RCV000083438.1,