rs72558488

Orientation

plus

Stabilized

plus

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

Make rs72558488(C;C)

Make rs72558488(C;G)

Reference

GRCh38 38.1/141

Chromosome

X

Position

38421032

Gene

OTC

is a	snp
is	mentioned by
dbSNP	rs72558488
dbSNP (classic)	rs72558488
ClinGen	rs72558488
ebi	rs72558488
HLI	rs72558488
Exac	rs72558488
Gnomad	rs72558488
Varsome	rs72558488
LitVar	rs72558488
Map	rs72558488
PheGenI	rs72558488
Biobank	rs72558488
1000 genomes	rs72558488
hgdp	rs72558488
ensembl	rs72558488
geneview	rs72558488
scholar	rs72558488
google	rs72558488
pharmgkb	rs72558488
gwascentral	rs72558488
openSNP	rs72558488
23andMe	rs72558488
SNPshot	rs72558488
SNPdbe	rs72558488
MSV3d	rs72558488
GWAS Ctlg	rs72558488

Max Magnitude

0

ClinVar
Risk	rs72558488(C;C)
Alt	rs72558488(C;C)
Reference	Rs72558488(G;G)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	OTC
CLNDBN	not provided
Reversed	0
HGVS	NC_000023.10:g.38280285G>C
CLNSRC	UniProtKB (protein)
CLNACC	RCV000083320.1,