rs72558451

Orientation

plus

Stabilized

plus

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

Make rs72558451(C;T)

Make rs72558451(T;T)

Reference

GRCh38 38.1/141

Chromosome

X

Position

38408966

Gene

OTC

is a	snp
is	mentioned by
dbSNP	rs72558451
dbSNP (classic)	rs72558451
ClinGen	rs72558451
ebi	rs72558451
HLI	rs72558451
Exac	rs72558451
Gnomad	rs72558451
Varsome	rs72558451
LitVar	rs72558451
Map	rs72558451
PheGenI	rs72558451
Biobank	rs72558451
1000 genomes	rs72558451
hgdp	rs72558451
ensembl	rs72558451
geneview	rs72558451
scholar	rs72558451
google	rs72558451
pharmgkb	rs72558451
gwascentral	rs72558451
openSNP	rs72558451
23andMe	rs72558451
SNPshot	rs72558451
SNPdbe	rs72558451
MSV3d	rs72558451
GWAS Ctlg	rs72558451

Max Magnitude

0

ClinVar
Risk	rs72558451(G;G) rs72558451(T;T)
Alt	rs72558451(G;G) rs72558451(T;T)
Reference	Rs72558451(C;C)
Significance	Pathogenic
Disease	not specified not provided
Variation	info
Gene	OTC
CLNDBN	not specified not provided
Reversed	0
HGVS	NC_000023.10:g.38268219C>G; NC_000023.10:g.38268219C>T
CLNSRC	ClinVar Emory University
CLNACC	RCV000079088.4, RCV000083582.1,