rs72556296

Orientation

plus

Stabilized

plus

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

Make rs72556296(C;T)

Make rs72556296(T;T)

Reference

GRCh38 38.1/141

Chromosome

X

Position

38403648

Gene

OTC

is a	snp
is	mentioned by
dbSNP	rs72556296
dbSNP (classic)	rs72556296
ClinGen	rs72556296
ebi	rs72556296
HLI	rs72556296
Exac	rs72556296
Gnomad	rs72556296
Varsome	rs72556296
LitVar	rs72556296
Map	rs72556296
PheGenI	rs72556296
Biobank	rs72556296
1000 genomes	rs72556296
hgdp	rs72556296
ensembl	rs72556296
geneview	rs72556296
scholar	rs72556296
google	rs72556296
pharmgkb	rs72556296
gwascentral	rs72556296
openSNP	rs72556296
23andMe	rs72556296
SNPshot	rs72556296
SNPdbe	rs72556296
MSV3d	rs72556296
GWAS Ctlg	rs72556296

Max Magnitude

0

ClinVar
Risk	rs72556296(T;T)
Alt	rs72556296(T;T)
Reference	Rs72556296(C;C)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	OTC
CLNDBN	not provided
Reversed	0
HGVS	NC_000023.10:g.38262901C>T
CLNSRC	UniProtKB (protein)
CLNACC	RCV000083491.1,