rs72558443

Orientation

plus

Stabilized

plus

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

Make rs72558443(A;G)

Make rs72558443(G;G)

Reference

GRCh38 38.1/141

Chromosome

X

Position

38408946

Gene

OTC

is a	snp
is	mentioned by
dbSNP	rs72558443
dbSNP (classic)	rs72558443
ClinGen	rs72558443
ebi	rs72558443
HLI	rs72558443
Exac	rs72558443
Gnomad	rs72558443
Varsome	rs72558443
LitVar	rs72558443
Map	rs72558443
PheGenI	rs72558443
Biobank	rs72558443
1000 genomes	rs72558443
hgdp	rs72558443
ensembl	rs72558443
geneview	rs72558443
scholar	rs72558443
google	rs72558443
pharmgkb	rs72558443
gwascentral	rs72558443
openSNP	rs72558443
23andMe	rs72558443
SNPshot	rs72558443
SNPdbe	rs72558443
MSV3d	rs72558443
GWAS Ctlg	rs72558443

Max Magnitude

0

ClinVar
Risk	rs72558443(G;G)
Alt	rs72558443(G;G)
Reference	Rs72558443(A;A)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	OTC
CLNDBN	not provided
Reversed	0
HGVS	NC_000023.10:g.38268199A>G
CLNSRC	UniProtKB (protein)
CLNACC	RCV000083572.1,