rs72558475

Orientation

plus

Stabilized

plus

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

Make rs72558475(A;A)

Make rs72558475(A;C)

Reference

GRCh38 38.1/141

Chromosome

X

Position

38411956

Gene

OTC

is a	snp
is	mentioned by
dbSNP	rs72558475
dbSNP (classic)	rs72558475
ClinGen	rs72558475
ebi	rs72558475
HLI	rs72558475
Exac	rs72558475
Gnomad	rs72558475
Varsome	rs72558475
LitVar	rs72558475
Map	rs72558475
PheGenI	rs72558475
Biobank	rs72558475
1000 genomes	rs72558475
hgdp	rs72558475
ensembl	rs72558475
geneview	rs72558475
scholar	rs72558475
google	rs72558475
pharmgkb	rs72558475
gwascentral	rs72558475
openSNP	rs72558475
23andMe	rs72558475
SNPshot	rs72558475
SNPdbe	rs72558475
MSV3d	rs72558475
GWAS Ctlg	rs72558475

Max Magnitude

0

ClinVar
Risk	rs72558475(A;A)
Alt	rs72558475(A;A)
Reference	Rs72558475(C;C)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	OTC
CLNDBN	not provided
Reversed	0
HGVS	NC_000023.10:g.38271209C>A
CLNSRC	ClinVar
CLNACC	RCV000083622.1,