rs72558453

Orientation

plus

Stabilized

plus

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

Make rs72558453(-;-)

Make rs72558453(-;A)

Reference

GRCh38 38.1/141

Chromosome

X

Position

38408976

Gene

OTC

is a	snp
is	mentioned by
dbSNP	rs72558453
dbSNP (classic)	rs72558453
ClinGen	rs72558453
ebi	rs72558453
HLI	rs72558453
Exac	rs72558453
Gnomad	rs72558453
Varsome	rs72558453
LitVar	rs72558453
Map	rs72558453
PheGenI	rs72558453
Biobank	rs72558453
1000 genomes	rs72558453
hgdp	rs72558453
ensembl	rs72558453
geneview	rs72558453
scholar	rs72558453
google	rs72558453
pharmgkb	rs72558453
gwascentral	rs72558453
openSNP	rs72558453
23andMe	rs72558453
SNPshot	rs72558453
SNPdbe	rs72558453
MSV3d	rs72558453
GWAS Ctlg	rs72558453

Max Magnitude

0

ClinVar
Risk	rs72558453(-;-)
Alt	rs72558453(-;-)
Reference	Rs72558453(A;A)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	OTC
CLNDBN	not provided
Reversed	0
HGVS	NC_000023.10:g.38268229delA
CLNSRC	ClinVar
CLNACC	RCV000083585.1,