rs72556268

Orientation

plus

Stabilized

plus

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

Make rs72556268(A;A)

Make rs72556268(A;C)

Reference

GRCh38 38.1/141

Chromosome

X

Position

38401352

Gene

OTC

is a	snp
is	mentioned by
dbSNP	rs72556268
dbSNP (classic)	rs72556268
ClinGen	rs72556268
ebi	rs72556268
HLI	rs72556268
Exac	rs72556268
Gnomad	rs72556268
Varsome	rs72556268
LitVar	rs72556268
Map	rs72556268
PheGenI	rs72556268
Biobank	rs72556268
1000 genomes	rs72556268
hgdp	rs72556268
ensembl	rs72556268
geneview	rs72556268
scholar	rs72556268
google	rs72556268
pharmgkb	rs72556268
gwascentral	rs72556268
openSNP	rs72556268
23andMe	rs72556268
SNPshot	rs72556268
SNPdbe	rs72556268
MSV3d	rs72556268
GWAS Ctlg	rs72556268

Max Magnitude

0

ClinVar
Risk	rs72556268(A;A)
Alt	rs72556268(A;A)
Reference	Rs72556268(C;C)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	OTC
CLNDBN	not provided
Reversed	0
HGVS	NC_000023.10:g.38260605C>A
CLNSRC	ClinVar
CLNACC	RCV000083449.1,