rs72558409

Orientation

plus

Stabilized

plus

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

Make rs72558409(A;C)

Make rs72558409(C;C)

Reference

GRCh38 38.1/141

Chromosome

X

Position

38403682

Gene

OTC

is a	snp
is	mentioned by
dbSNP	rs72558409
dbSNP (classic)	rs72558409
ClinGen	rs72558409
ebi	rs72558409
HLI	rs72558409
Exac	rs72558409
Gnomad	rs72558409
Varsome	rs72558409
LitVar	rs72558409
Map	rs72558409
PheGenI	rs72558409
Biobank	rs72558409
1000 genomes	rs72558409
hgdp	rs72558409
ensembl	rs72558409
geneview	rs72558409
scholar	rs72558409
google	rs72558409
pharmgkb	rs72558409
gwascentral	rs72558409
openSNP	rs72558409
23andMe	rs72558409
SNPshot	rs72558409
SNPdbe	rs72558409
MSV3d	rs72558409
GWAS Ctlg	rs72558409

Max Magnitude

0

ClinVar
Risk	rs72558409(C;C)
Alt	rs72558409(C;C)
Reference	Rs72558409(A;A)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	OTC
CLNDBN	not provided
Reversed	0
HGVS	NC_000023.10:g.38262935A>C
CLNSRC	ClinVar
CLNACC	RCV000083510.1,