rs72556290

Orientation

plus

Stabilized

plus

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

Make rs72556290(A;G)

Make rs72556290(G;G)

Reference

GRCh38 38.1/141

Chromosome

X

Position

38403619

Gene

OTC

is a	snp
is	mentioned by
dbSNP	rs72556290
dbSNP (classic)	rs72556290
ClinGen	rs72556290
ebi	rs72556290
HLI	rs72556290
Exac	rs72556290
Gnomad	rs72556290
Varsome	rs72556290
LitVar	rs72556290
Map	rs72556290
PheGenI	rs72556290
Biobank	rs72556290
1000 genomes	rs72556290
hgdp	rs72556290
ensembl	rs72556290
geneview	rs72556290
scholar	rs72556290
google	rs72556290
pharmgkb	rs72556290
gwascentral	rs72556290
openSNP	rs72556290
23andMe	rs72556290
SNPshot	rs72556290
SNPdbe	rs72556290
MSV3d	rs72556290
GWAS Ctlg	rs72556290

Max Magnitude

0

ClinVar
Risk	rs72556290(G;G)
Alt	rs72556290(G;G)
Reference	Rs72556290(A;A)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	OTC
CLNDBN	not provided
Reversed	0
HGVS	NC_000023.10:g.38262872A>G
CLNSRC	UniProtKB (protein)
CLNACC	RCV000083485.1,