rs72558477

Orientation

plus

Stabilized

plus

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

Make rs72558477(G;T)

Make rs72558477(T;T)

Reference

GRCh38 38.1/141

Chromosome

X

Position

38411976

Gene

OTC

is a	snp
is	mentioned by
dbSNP	rs72558477
dbSNP (classic)	rs72558477
ClinGen	rs72558477
ebi	rs72558477
HLI	rs72558477
Exac	rs72558477
Gnomad	rs72558477
Varsome	rs72558477
LitVar	rs72558477
Map	rs72558477
PheGenI	rs72558477
Biobank	rs72558477
1000 genomes	rs72558477
hgdp	rs72558477
ensembl	rs72558477
geneview	rs72558477
scholar	rs72558477
google	rs72558477
pharmgkb	rs72558477
gwascentral	rs72558477
openSNP	rs72558477
23andMe	rs72558477
SNPshot	rs72558477
SNPdbe	rs72558477
MSV3d	rs72558477
GWAS Ctlg	rs72558477

Max Magnitude

0

ClinVar
Risk	rs72558477(T;T)
Alt	rs72558477(T;T)
Reference	Rs72558477(G;G)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	OTC
CLNDBN	not provided
Reversed	0
HGVS	NC_000023.10:g.38271229G>T
CLNSRC	ClinVar
CLNACC	RCV000083624.1,