rs111060773

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(AGGTA;AGGTA)	0	common in clinvar
(GTAAG;GTAAG)	0	common in clinvar

Make rs111060773(-;-)

Make rs111060773(-;GTAAG)

Reference

GRCh38 38.1/141

Chromosome

X

Position

38369878

Gene

OTC

is a	snp
is	mentioned by
dbSNP	rs111060773
dbSNP (classic)	rs111060773
ClinGen	rs111060773
ebi	rs111060773
HLI	rs111060773
Exac	rs111060773
Gnomad	rs111060773
Varsome	rs111060773
LitVar	rs111060773
Map	rs111060773
PheGenI	rs111060773
Biobank	rs111060773
1000 genomes	rs111060773
hgdp	rs111060773
ensembl	rs111060773
geneview	rs111060773
scholar	rs111060773
google	rs111060773
pharmgkb	rs111060773
gwascentral	rs111060773
openSNP	rs111060773
23andMe	rs111060773
SNPshot	rs111060773
SNPdbe	rs111060773
MSV3d	rs111060773
GWAS Ctlg	rs111060773

Max Magnitude

0

ClinVar
Risk	rs111060773(-;-)
Alt	rs111060773(-;-)
Reference	Rs111060773(AGGTA;AGGTA)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	OTC
CLNDBN	not provided
Reversed	0
HGVS	NC_000023.10:g.38229131_38229135delGTAAG
CLNSRC	ClinVar
CLNACC	RCV000083394.1,