rs72556274

Orientation

plus

Stabilized

plus

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

Make rs72556274(C;G)

Make rs72556274(G;G)

Reference

GRCh38 38.1/141

Chromosome

X

Position

38401379

Gene

OTC

is a	snp
is	mentioned by
dbSNP	rs72556274
dbSNP (classic)	rs72556274
ClinGen	rs72556274
ebi	rs72556274
HLI	rs72556274
Exac	rs72556274
Gnomad	rs72556274
Varsome	rs72556274
LitVar	rs72556274
Map	rs72556274
PheGenI	rs72556274
Biobank	rs72556274
1000 genomes	rs72556274
hgdp	rs72556274
ensembl	rs72556274
geneview	rs72556274
scholar	rs72556274
google	rs72556274
pharmgkb	rs72556274
gwascentral	rs72556274
openSNP	rs72556274
23andMe	rs72556274
SNPshot	rs72556274
SNPdbe	rs72556274
MSV3d	rs72556274
GWAS Ctlg	rs72556274

Max Magnitude

0

ClinVar
Risk	rs72556274(G;G)
Alt	rs72556274(G;G)
Reference	Rs72556274(C;C)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	OTC
CLNDBN	not provided
Reversed	0
HGVS	NC_000023.10:g.38260632C>G
CLNSRC	ClinVar
CLNACC	RCV000083460.1,