rs72556289

Orientation

plus

Stabilized

plus

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

Make rs72556289(A;G)

Make rs72556289(G;G)

Reference

GRCh38 38.1/141

Chromosome

X

Position

38403616

Gene

OTC

is a	snp
is	mentioned by
dbSNP	rs72556289
dbSNP (classic)	rs72556289
ClinGen	rs72556289
ebi	rs72556289
HLI	rs72556289
Exac	rs72556289
Gnomad	rs72556289
Varsome	rs72556289
LitVar	rs72556289
Map	rs72556289
PheGenI	rs72556289
Biobank	rs72556289
1000 genomes	rs72556289
hgdp	rs72556289
ensembl	rs72556289
geneview	rs72556289
scholar	rs72556289
google	rs72556289
pharmgkb	rs72556289
gwascentral	rs72556289
openSNP	rs72556289
23andMe	rs72556289
SNPshot	rs72556289
SNPdbe	rs72556289
MSV3d	rs72556289
GWAS Ctlg	rs72556289

Max Magnitude

0

ClinVar
Risk	rs72556289(G;G)
Alt	rs72556289(G;G)
Reference	Rs72556289(A;A)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	OTC
CLNDBN	not provided
Reversed	0
HGVS	NC_000023.10:g.38262869A>G
CLNSRC	ClinVar
CLNACC	RCV000083484.1,