rs796052016

Orientation

plus

Stabilized

plus

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

Make rs796052016(-;-)

Make rs796052016(-;GG)

Reference

GRCh38.p2 38.2/147

Chromosome

X

Position

38403639

Gene

OTC

is a	snp
is	mentioned by
dbSNP	rs796052016
dbSNP (classic)	rs796052016
ClinGen	rs796052016
ebi	rs796052016
HLI	rs796052016
Exac	rs796052016
Gnomad	rs796052016
Varsome	rs796052016
LitVar	rs796052016
Map	rs796052016
PheGenI	rs796052016
Biobank	rs796052016
1000 genomes	rs796052016
hgdp	rs796052016
ensembl	rs796052016
geneview	rs796052016
scholar	rs796052016
google	rs796052016
pharmgkb	rs796052016
gwascentral	rs796052016
openSNP	rs796052016
23andMe	rs796052016
SNPshot	rs796052016
SNPdbe	rs796052016
MSV3d	rs796052016
GWAS Ctlg	rs796052016

Max Magnitude

0

ClinVar
Risk	rs796052016(-;-)
Alt	rs796052016(-;-)
Reference	Rs796052016(GG;GG)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	OTC
CLNDBN	not provided
Reversed	0
HGVS	NC_000023.10:g.38262892_38262893delGG
CLNSRC
CLNACC	RCV000186071.1,