rs72558460

Orientation

plus

Stabilized

plus

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

Make rs72558460(-;-)

Make rs72558460(-;TG)

Reference

GRCh38 38.1/141

Chromosome

X

Position

38411886

Gene

OTC

is a	snp
is	mentioned by
dbSNP	rs72558460
dbSNP (classic)	rs72558460
ClinGen	rs72558460
ebi	rs72558460
HLI	rs72558460
Exac	rs72558460
Gnomad	rs72558460
Varsome	rs72558460
LitVar	rs72558460
Map	rs72558460
PheGenI	rs72558460
Biobank	rs72558460
1000 genomes	rs72558460
hgdp	rs72558460
ensembl	rs72558460
geneview	rs72558460
scholar	rs72558460
google	rs72558460
pharmgkb	rs72558460
gwascentral	rs72558460
openSNP	rs72558460
23andMe	rs72558460
SNPshot	rs72558460
SNPdbe	rs72558460
MSV3d	rs72558460
GWAS Ctlg	rs72558460

Max Magnitude

0

ClinVar
Risk	rs72558460(-;-)
Alt	rs72558460(-;-)
Reference	Rs72558460(TG;TG)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	OTC
CLNDBN	not provided
Reversed	0
HGVS	NC_000023.10:g.38271139_38271140delTG
CLNSRC	ClinVar
CLNACC	RCV000083596.1,