rs72558456

Orientation

plus

Stabilized

plus

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

Make rs72558456(G;T)

Make rs72558456(T;T)

Reference

GRCh38 38.1/141

Chromosome

X

Position

38409025

Gene

OTC

is a	snp
is	mentioned by
dbSNP	rs72558456
dbSNP (classic)	rs72558456
ClinGen	rs72558456
ebi	rs72558456
HLI	rs72558456
Exac	rs72558456
Gnomad	rs72558456
Varsome	rs72558456
LitVar	rs72558456
Map	rs72558456
PheGenI	rs72558456
Biobank	rs72558456
1000 genomes	rs72558456
hgdp	rs72558456
ensembl	rs72558456
geneview	rs72558456
scholar	rs72558456
google	rs72558456
pharmgkb	rs72558456
gwascentral	rs72558456
openSNP	rs72558456
23andMe	rs72558456
SNPshot	rs72558456
SNPdbe	rs72558456
MSV3d	rs72558456
GWAS Ctlg	rs72558456

Max Magnitude

0

ClinVar
Risk	rs72558456(T;T)
Alt	rs72558456(T;T)
Reference	Rs72558456(G;G)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	OTC
CLNDBN	not provided
Reversed	0
HGVS	NC_000023.10:g.38268278G>T
CLNSRC	ClinVar
CLNACC	RCV000083592.1,