rs72556272

Orientation

plus

Stabilized

plus

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

Make rs72556272(A;A)

Make rs72556272(A;G)

Reference

GRCh38 38.1/141

Chromosome

X

Position

38401373

Gene

OTC

is a	snp
is	mentioned by
dbSNP	rs72556272
dbSNP (classic)	rs72556272
ClinGen	rs72556272
ebi	rs72556272
HLI	rs72556272
Exac	rs72556272
Gnomad	rs72556272
Varsome	rs72556272
LitVar	rs72556272
Map	rs72556272
PheGenI	rs72556272
Biobank	rs72556272
1000 genomes	rs72556272
hgdp	rs72556272
ensembl	rs72556272
geneview	rs72556272
scholar	rs72556272
google	rs72556272
pharmgkb	rs72556272
gwascentral	rs72556272
openSNP	rs72556272
23andMe	rs72556272
SNPshot	rs72556272
SNPdbe	rs72556272
MSV3d	rs72556272
GWAS Ctlg	rs72556272

Max Magnitude

0

ClinVar
Risk	rs72556272(A;A)
Alt	rs72556272(A;A)
Reference	Rs72556272(G;G)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	OTC
CLNDBN	not provided
Reversed	0
HGVS	NC_000023.10:g.38260626G>A
CLNSRC	ClinVar
CLNACC	RCV000083458.1,