rs72558492

Orientation

plus

Stabilized

plus

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

Make rs72558492(A;G)

Make rs72558492(G;G)

Reference

GRCh38 38.1/141

Chromosome

X

Position

38421051

Gene

OTC

is a	snp
is	mentioned by
dbSNP	rs72558492
dbSNP (classic)	rs72558492
ClinGen	rs72558492
ebi	rs72558492
HLI	rs72558492
Exac	rs72558492
Gnomad	rs72558492
Varsome	rs72558492
LitVar	rs72558492
Map	rs72558492
PheGenI	rs72558492
Biobank	rs72558492
1000 genomes	rs72558492
hgdp	rs72558492
ensembl	rs72558492
geneview	rs72558492
scholar	rs72558492
google	rs72558492
pharmgkb	rs72558492
gwascentral	rs72558492
openSNP	rs72558492
23andMe	rs72558492
SNPshot	rs72558492
SNPdbe	rs72558492
MSV3d	rs72558492
GWAS Ctlg	rs72558492

Max Magnitude

0

ClinVar
Risk	rs72558492(G;G)
Alt	rs72558492(G;G)
Reference	Rs72558492(A;A)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	OTC
CLNDBN	not provided
Reversed	0
HGVS	NC_000023.10:g.38280304A>G
CLNSRC	UniProtKB (protein)
CLNACC	RCV000083326.1,