rs72558485

Orientation

plus

Stabilized

plus

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

Make rs72558485(C;G)

Make rs72558485(G;G)

Reference

GRCh38 38.1/141

Chromosome

X

Position

38421020

Gene

OTC

is a	snp
is	mentioned by
dbSNP	rs72558485
dbSNP (classic)	rs72558485
ClinGen	rs72558485
ebi	rs72558485
HLI	rs72558485
Exac	rs72558485
Gnomad	rs72558485
Varsome	rs72558485
LitVar	rs72558485
Map	rs72558485
PheGenI	rs72558485
Biobank	rs72558485
1000 genomes	rs72558485
hgdp	rs72558485
ensembl	rs72558485
geneview	rs72558485
scholar	rs72558485
google	rs72558485
pharmgkb	rs72558485
gwascentral	rs72558485
openSNP	rs72558485
23andMe	rs72558485
SNPshot	rs72558485
SNPdbe	rs72558485
MSV3d	rs72558485
GWAS Ctlg	rs72558485

Max Magnitude

0

ClinVar
Risk	rs72558485(G;G)
Alt	rs72558485(G;G)
Reference	Rs72558485(C;C)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	OTC
CLNDBN	not provided
Reversed	0
HGVS	NC_000023.10:g.38280273C>G
CLNSRC	ClinVar
CLNACC	RCV000083317.1,