rs72556293

Orientation

plus

Stabilized

plus

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

Make rs72556293(A;G)

Make rs72556293(G;G)

Reference

GRCh38 38.1/141

Chromosome

X

Position

38403625

Gene

OTC

is a	snp
is	mentioned by
dbSNP	rs72556293
dbSNP (classic)	rs72556293
ClinGen	rs72556293
ebi	rs72556293
HLI	rs72556293
Exac	rs72556293
Gnomad	rs72556293
Varsome	rs72556293
LitVar	rs72556293
Map	rs72556293
PheGenI	rs72556293
Biobank	rs72556293
1000 genomes	rs72556293
hgdp	rs72556293
ensembl	rs72556293
geneview	rs72556293
scholar	rs72556293
google	rs72556293
pharmgkb	rs72556293
gwascentral	rs72556293
openSNP	rs72556293
23andMe	rs72556293
SNPshot	rs72556293
SNPdbe	rs72556293
MSV3d	rs72556293
GWAS Ctlg	rs72556293

Max Magnitude

0

ClinVar
Risk	rs72556293(G;G)
Alt	rs72556293(G;G)
Reference	Rs72556293(A;A)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	OTC
CLNDBN	not provided
Reversed	0
HGVS	NC_000023.10:g.38262878A>G
CLNSRC	UniProtKB (protein)
CLNACC	RCV000083488.1,