rs67870245

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(C;C)	0	common in clinvar

Make rs67870245(-;-)

Make rs67870245(-;C)

Reference

GRCh38 38.1/141

Chromosome

X

Position

38411900

Gene

OTC

is a	snp
is	mentioned by
dbSNP	rs67870245
dbSNP (classic)	rs67870245
ClinGen	rs67870245
ebi	rs67870245
HLI	rs67870245
Exac	rs67870245
Gnomad	rs67870245
Varsome	rs67870245
LitVar	rs67870245
Map	rs67870245
PheGenI	rs67870245
Biobank	rs67870245
1000 genomes	rs67870245
hgdp	rs67870245
ensembl	rs67870245
geneview	rs67870245
scholar	rs67870245
google	rs67870245
pharmgkb	rs67870245
gwascentral	rs67870245
openSNP	rs67870245
23andMe	rs67870245
SNPshot	rs67870245
SNPdbe	rs67870245
MSV3d	rs67870245
GWAS Ctlg	rs67870245

Max Magnitude

0

ClinVar
Risk	rs67870245(-;-)
Alt	rs67870245(-;-)
Reference	Rs67870245(C;C)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	OTC
CLNDBN	not provided
Reversed	0
HGVS	NC_000023.10:g.38271153delC
CLNSRC	ClinVar
CLNACC	RCV000083603.1,