rs72558455

Orientation

plus

Stabilized

plus

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

Make rs72558455(C;T)

Make rs72558455(T;T)

Reference

GRCh38 38.1/141

Chromosome

X

Position

38408993

Gene

OTC

is a	snp
is	mentioned by
dbSNP	rs72558455
dbSNP (classic)	rs72558455
ClinGen	rs72558455
ebi	rs72558455
HLI	rs72558455
Exac	rs72558455
Gnomad	rs72558455
Varsome	rs72558455
LitVar	rs72558455
Map	rs72558455
PheGenI	rs72558455
Biobank	rs72558455
1000 genomes	rs72558455
hgdp	rs72558455
ensembl	rs72558455
geneview	rs72558455
scholar	rs72558455
google	rs72558455
pharmgkb	rs72558455
gwascentral	rs72558455
openSNP	rs72558455
23andMe	rs72558455
SNPshot	rs72558455
SNPdbe	rs72558455
MSV3d	rs72558455
GWAS Ctlg	rs72558455

Max Magnitude

0

ClinVar
Risk	rs72558455(T;T)
Alt	rs72558455(T;T)
Reference	Rs72558455(C;C)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	OTC
CLNDBN	not provided
Reversed	0
HGVS	NC_000023.10:g.38268246C>T
CLNSRC	ClinVar
CLNACC	RCV000083589.1,