rs72558461

Orientation

plus

Stabilized

plus

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

Make rs72558461(C;C)

Make rs72558461(C;G)

Reference

GRCh38 38.1/141

Chromosome

X

Position

38411887

Gene

OTC

is a	snp
is	mentioned by
dbSNP	rs72558461
dbSNP (classic)	rs72558461
ClinGen	rs72558461
ebi	rs72558461
HLI	rs72558461
Exac	rs72558461
Gnomad	rs72558461
Varsome	rs72558461
LitVar	rs72558461
Map	rs72558461
PheGenI	rs72558461
Biobank	rs72558461
1000 genomes	rs72558461
hgdp	rs72558461
ensembl	rs72558461
geneview	rs72558461
scholar	rs72558461
google	rs72558461
pharmgkb	rs72558461
gwascentral	rs72558461
openSNP	rs72558461
23andMe	rs72558461
SNPshot	rs72558461
SNPdbe	rs72558461
MSV3d	rs72558461
GWAS Ctlg	rs72558461

Max Magnitude

0

ClinVar
Risk	rs72558461(C;C)
Alt	rs72558461(C;C)
Reference	Rs72558461(G;G)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	OTC
CLNDBN	not provided
Reversed	0
HGVS	NC_000023.10:g.38271140G>C
CLNSRC	ClinVar
CLNACC	RCV000083597.1,