rs72556273

Orientation

plus

Stabilized

plus

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

Make rs72556273(C;C)

Make rs72556273(C;T)

Reference

GRCh38 38.1/141

Chromosome

X

Position

38401378

Gene

OTC

is a	snp
is	mentioned by
dbSNP	rs72556273
dbSNP (classic)	rs72556273
ClinGen	rs72556273
ebi	rs72556273
HLI	rs72556273
Exac	rs72556273
Gnomad	rs72556273
Varsome	rs72556273
LitVar	rs72556273
Map	rs72556273
PheGenI	rs72556273
Biobank	rs72556273
1000 genomes	rs72556273
hgdp	rs72556273
ensembl	rs72556273
geneview	rs72556273
scholar	rs72556273
google	rs72556273
pharmgkb	rs72556273
gwascentral	rs72556273
openSNP	rs72556273
23andMe	rs72556273
SNPshot	rs72556273
SNPdbe	rs72556273
MSV3d	rs72556273
GWAS Ctlg	rs72556273

Max Magnitude

0

ClinVar
Risk	rs72556273(C;C)
Alt	rs72556273(C;C)
Reference	Rs72556273(T;T)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	OTC
CLNDBN	not provided
Reversed	0
HGVS	NC_000023.10:g.38260631T>C
CLNSRC	ClinVar
CLNACC	RCV000083459.1,