rs72552298

Orientation

plus

Stabilized

plus

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

Make rs72552298(-;-)

Make rs72552298(-;T)

Reference

GRCh38 38.1/141

Chromosome

X

Position

38352736

Gene

OTC

is a	snp
is	mentioned by
dbSNP	rs72552298
dbSNP (classic)	rs72552298
ClinGen	rs72552298
ebi	rs72552298
HLI	rs72552298
Exac	rs72552298
Gnomad	rs72552298
Varsome	rs72552298
LitVar	rs72552298
Map	rs72552298
PheGenI	rs72552298
Biobank	rs72552298
1000 genomes	rs72552298
hgdp	rs72552298
ensembl	rs72552298
geneview	rs72552298
scholar	rs72552298
google	rs72552298
pharmgkb	rs72552298
gwascentral	rs72552298
openSNP	rs72552298
23andMe	rs72552298
SNPshot	rs72552298
SNPdbe	rs72552298
MSV3d	rs72552298
GWAS Ctlg	rs72552298

Max Magnitude

0

ClinVar
Risk	rs72552298(-;-)
Alt	rs72552298(-;-)
Reference	Rs72552298(T;T)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	OTC
CLNDBN	not provided
Reversed	0
HGVS	NC_000023.10:g.38211989delT
CLNSRC	ClinVar
CLNACC	RCV000083429.1,