rs72558464

Orientation

plus

Stabilized

plus

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

Make rs72558464(A;A)

Make rs72558464(A;G)

Reference

GRCh38 38.1/141

Chromosome

X

Position

38411902

Gene

OTC

is a	snp
is	mentioned by
dbSNP	rs72558464
dbSNP (classic)	rs72558464
ClinGen	rs72558464
ebi	rs72558464
HLI	rs72558464
Exac	rs72558464
Gnomad	rs72558464
Varsome	rs72558464
LitVar	rs72558464
Map	rs72558464
PheGenI	rs72558464
Biobank	rs72558464
1000 genomes	rs72558464
hgdp	rs72558464
ensembl	rs72558464
geneview	rs72558464
scholar	rs72558464
google	rs72558464
pharmgkb	rs72558464
gwascentral	rs72558464
openSNP	rs72558464
23andMe	rs72558464
SNPshot	rs72558464
SNPdbe	rs72558464
MSV3d	rs72558464
GWAS Ctlg	rs72558464

Max Magnitude

0

ClinVar
Risk	rs72558464(A;A)
Alt	rs72558464(A;A)
Reference	Rs72558464(G;G)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	OTC
CLNDBN	not provided
Reversed	0
HGVS	NC_000023.10:g.38271155G>A
CLNSRC	UniProtKB (protein)
CLNACC	RCV000083606.1,