rs72558452

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(GAG;GAG)	0	common in clinvar
(I;I)	0

Make rs72558452(-;-)

Make rs72558452(-;GAG)

Reference

GRCh38 38.1/141

Chromosome

X

Position

38408975

Gene

OTC

is a	snp
is	mentioned by
dbSNP	rs72558452
dbSNP (classic)	rs72558452
ClinGen	rs72558452
ebi	rs72558452
HLI	rs72558452
Exac	rs72558452
Gnomad	rs72558452
Varsome	rs72558452
LitVar	rs72558452
Map	rs72558452
PheGenI	rs72558452
Biobank	rs72558452
1000 genomes	rs72558452
hgdp	rs72558452
ensembl	rs72558452
geneview	rs72558452
scholar	rs72558452
google	rs72558452
pharmgkb	rs72558452
gwascentral	rs72558452
openSNP	rs72558452
23andMe	rs72558452
SNPshot	rs72558452
SNPdbe	rs72558452
MSV3d	rs72558452
GWAS Ctlg	rs72558452

Max Magnitude

0

ClinVar
Risk	rs72558452(-;-)
Alt	rs72558452(-;-)
Reference	Rs72558452(GAG;GAG)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	OTC
CLNDBN	not provided
Reversed	0
HGVS	NC_000023.10:g.38268228_38268230delGAG
CLNSRC	ClinVar
CLNACC	RCV000083584.1,