rs72558440

Orientation

plus

Stabilized

plus

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

Make rs72558440(A;C)

Make rs72558440(C;C)

Reference

GRCh38 38.1/141

Chromosome

X

Position

38408922

Gene

OTC

is a	snp
is	mentioned by
dbSNP	rs72558440
dbSNP (classic)	rs72558440
ClinGen	rs72558440
ebi	rs72558440
HLI	rs72558440
Exac	rs72558440
Gnomad	rs72558440
Varsome	rs72558440
LitVar	rs72558440
Map	rs72558440
PheGenI	rs72558440
Biobank	rs72558440
1000 genomes	rs72558440
hgdp	rs72558440
ensembl	rs72558440
geneview	rs72558440
scholar	rs72558440
google	rs72558440
pharmgkb	rs72558440
gwascentral	rs72558440
openSNP	rs72558440
23andMe	rs72558440
SNPshot	rs72558440
SNPdbe	rs72558440
MSV3d	rs72558440
GWAS Ctlg	rs72558440

Max Magnitude

0

ClinVar
Risk	rs72558440(C;C) rs72558440(G;G)
Alt	rs72558440(C;C) rs72558440(G;G)
Reference	Rs72558440(A;A)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	OTC
CLNDBN	not provided
Reversed	0
HGVS	NC_000023.10:g.38268175A>C
CLNSRC	UniProtKB (protein)
CLNACC	RCV000083558.1,