rs67839039

Orientation

plus

Stabilized

plus

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

Make rs67839039(-;-)

Make rs67839039(-;G)

Reference

GRCh38 38.1/141

Chromosome

X

Position

38408741

Gene

OTC

is a	snp
is	mentioned by
dbSNP	rs67839039
dbSNP (classic)	rs67839039
ClinGen	rs67839039
ebi	rs67839039
HLI	rs67839039
Exac	rs67839039
Gnomad	rs67839039
Varsome	rs67839039
LitVar	rs67839039
Map	rs67839039
PheGenI	rs67839039
Biobank	rs67839039
1000 genomes	rs67839039
hgdp	rs67839039
ensembl	rs67839039
geneview	rs67839039
scholar	rs67839039
google	rs67839039
pharmgkb	rs67839039
gwascentral	rs67839039
openSNP	rs67839039
23andMe	rs67839039
SNPshot	rs67839039
SNPdbe	rs67839039
MSV3d	rs67839039
GWAS Ctlg	rs67839039

Max Magnitude

0

ClinVar
Risk	rs67839039(-;-)
Alt	rs67839039(-;-)
Reference	Rs67839039(G;G)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	OTC
CLNDBN	not provided
Reversed	0
HGVS	NC_000023.10:g.38267994delG
CLNSRC	ClinVar
CLNACC	RCV000083533.1,