rs72558496

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(AAGT;AAGT)	0	common in clinvar
(GTAA;GTAA)	0	common in clinvar
(I;I)	0

Make rs72558496(-;-)

Make rs72558496(-;AAGT)

Reference

GRCh38 38.1/141

Chromosome

X

Position

38352776

Gene

OTC

is a	snp
is	mentioned by
dbSNP	rs72558496
dbSNP (classic)	rs72558496
ClinGen	rs72558496
ebi	rs72558496
HLI	rs72558496
Exac	rs72558496
Gnomad	rs72558496
Varsome	rs72558496
LitVar	rs72558496
Map	rs72558496
PheGenI	rs72558496
Biobank	rs72558496
1000 genomes	rs72558496
hgdp	rs72558496
ensembl	rs72558496
geneview	rs72558496
scholar	rs72558496
google	rs72558496
pharmgkb	rs72558496
gwascentral	rs72558496
openSNP	rs72558496
23andMe	rs72558496
SNPshot	rs72558496
SNPdbe	rs72558496
MSV3d	rs72558496
GWAS Ctlg	rs72558496

Max Magnitude

0

ClinVar
Risk	rs72558496(-;-)
Alt	rs72558496(-;-)
Reference	Rs72558496(GTAA;GTAA)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	OTC
CLNDBN	not provided
Reversed	0
HGVS	NC_000023.10:g.38212029_38212032delAAGT
CLNSRC	ClinVar
CLNACC	RCV000083561.1,