rs72556283

Orientation

plus

Stabilized

plus

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

Make rs72556283(A;G)

Make rs72556283(G;G)

Reference

GRCh38 38.1/141

Chromosome

X

Position

38401415

Gene

OTC

is a	snp
is	mentioned by
dbSNP	rs72556283
dbSNP (classic)	rs72556283
ClinGen	rs72556283
ebi	rs72556283
HLI	rs72556283
Exac	rs72556283
Gnomad	rs72556283
Varsome	rs72556283
LitVar	rs72556283
Map	rs72556283
PheGenI	rs72556283
Biobank	rs72556283
1000 genomes	rs72556283
hgdp	rs72556283
ensembl	rs72556283
geneview	rs72556283
scholar	rs72556283
google	rs72556283
pharmgkb	rs72556283
gwascentral	rs72556283
openSNP	rs72556283
23andMe	rs72556283
SNPshot	rs72556283
SNPdbe	rs72556283
MSV3d	rs72556283
GWAS Ctlg	rs72556283

Max Magnitude

0

ClinVar
Risk	rs72556283(G;G)
Alt	rs72556283(G;G)
Reference	Rs72556283(A;A)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	OTC
CLNDBN	not provided
Reversed	0
HGVS	NC_000023.10:g.38260668A>G
CLNSRC	UniProtKB (protein)
CLNACC	RCV000083475.1,