rs72556278

Orientation

plus

Stabilized

plus

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

Make rs72556278(C;T)

Make rs72556278(T;T)

Reference

GRCh38 38.1/141

Chromosome

X

Position

38401394

Gene

OTC

is a	snp
is	mentioned by
dbSNP	rs72556278
dbSNP (classic)	rs72556278
ClinGen	rs72556278
ebi	rs72556278
HLI	rs72556278
Exac	rs72556278
Gnomad	rs72556278
Varsome	rs72556278
LitVar	rs72556278
Map	rs72556278
PheGenI	rs72556278
Biobank	rs72556278
1000 genomes	rs72556278
hgdp	rs72556278
ensembl	rs72556278
geneview	rs72556278
scholar	rs72556278
google	rs72556278
pharmgkb	rs72556278
gwascentral	rs72556278
openSNP	rs72556278
23andMe	rs72556278
SNPshot	rs72556278
SNPdbe	rs72556278
MSV3d	rs72556278
GWAS Ctlg	rs72556278

Max Magnitude

0

ClinVar
Risk	rs72556278(T;T)
Alt	rs72556278(T;T)
Reference	Rs72556278(C;C)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	OTC
CLNDBN	not provided
Reversed	0
HGVS	NC_000023.10:g.38260647C>T
CLNSRC	ClinVar
CLNACC	RCV000083468.1,