rs72558469

Orientation

plus

Stabilized

plus

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

Make rs72558469(-;-)

Make rs72558469(-;GAA)

Reference

GRCh38 38.1/141

Chromosome

X

Position

38411934

Gene

OTC

is a	snp
is	mentioned by
dbSNP	rs72558469
dbSNP (classic)	rs72558469
ClinGen	rs72558469
ebi	rs72558469
HLI	rs72558469
Exac	rs72558469
Gnomad	rs72558469
Varsome	rs72558469
LitVar	rs72558469
Map	rs72558469
PheGenI	rs72558469
Biobank	rs72558469
1000 genomes	rs72558469
hgdp	rs72558469
ensembl	rs72558469
geneview	rs72558469
scholar	rs72558469
google	rs72558469
pharmgkb	rs72558469
gwascentral	rs72558469
openSNP	rs72558469
23andMe	rs72558469
SNPshot	rs72558469
SNPdbe	rs72558469
MSV3d	rs72558469
GWAS Ctlg	rs72558469

Max Magnitude

0

ClinVar
Risk	rs72558469(-;-)
Alt	rs72558469(-;-)
Reference	Rs72558469(GAA;GAA)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	OTC
CLNDBN	not provided
Reversed	0
HGVS	NC_000023.10:g.38271187_38271189delGAA
CLNSRC	ClinVar
CLNACC	RCV000083613.1,