rs72556284

Orientation

plus

Stabilized

plus

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

Make rs72556284(C;T)

Make rs72556284(T;T)

Reference

GRCh38 38.1/141

Chromosome

X

Position

38401421

Gene

OTC

is a	snp
is	mentioned by
dbSNP	rs72556284
dbSNP (classic)	rs72556284
ClinGen	rs72556284
ebi	rs72556284
HLI	rs72556284
Exac	rs72556284
Gnomad	rs72556284
Varsome	rs72556284
LitVar	rs72556284
Map	rs72556284
PheGenI	rs72556284
Biobank	rs72556284
1000 genomes	rs72556284
hgdp	rs72556284
ensembl	rs72556284
geneview	rs72556284
scholar	rs72556284
google	rs72556284
pharmgkb	rs72556284
gwascentral	rs72556284
openSNP	rs72556284
23andMe	rs72556284
SNPshot	rs72556284
SNPdbe	rs72556284
MSV3d	rs72556284
GWAS Ctlg	rs72556284

Max Magnitude

0

ClinVar
Risk	rs72556284(T;T)
Alt	rs72556284(T;T)
Reference	Rs72556284(C;C)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	OTC
CLNDBN	not provided
Reversed	0
HGVS	NC_000023.10:g.38260674C>T
CLNSRC	UniProtKB (protein)
CLNACC	RCV000083477.1,