rs72556253

Orientation

plus

Stabilized

plus

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

Make rs72556253(C;C)

Make rs72556253(C;T)

Reference

GRCh38 38.1/141

Chromosome

X

Position

38401282

Gene

OTC

is a	snp
is	mentioned by
dbSNP	rs72556253
dbSNP (classic)	rs72556253
ClinGen	rs72556253
ebi	rs72556253
HLI	rs72556253
Exac	rs72556253
Gnomad	rs72556253
Varsome	rs72556253
LitVar	rs72556253
Map	rs72556253
PheGenI	rs72556253
Biobank	rs72556253
1000 genomes	rs72556253
hgdp	rs72556253
ensembl	rs72556253
geneview	rs72556253
scholar	rs72556253
google	rs72556253
pharmgkb	rs72556253
gwascentral	rs72556253
openSNP	rs72556253
23andMe	rs72556253
SNPshot	rs72556253
SNPdbe	rs72556253
MSV3d	rs72556253
GWAS Ctlg	rs72556253

Max Magnitude

0

ClinVar
Risk	rs72556253(C;C)
Alt	rs72556253(C;C)
Reference	Rs72556253(T;T)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	OTC
CLNDBN	not provided
Reversed	0
HGVS	NC_000023.10:g.38260535T>C
CLNSRC	ClinVar
CLNACC	RCV000083422.1,