rs796052015

Orientation

plus

Stabilized

plus

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

Make rs796052015(-;A)

Make rs796052015(A;A)

Reference

GRCh38.p2 38.2/147

Chromosome

X

Position

38369794

Gene

OTC

is a	snp
is	mentioned by
dbSNP	rs796052015
dbSNP (classic)	rs796052015
ClinGen	rs796052015
ebi	rs796052015
HLI	rs796052015
Exac	rs796052015
Gnomad	rs796052015
Varsome	rs796052015
LitVar	rs796052015
Map	rs796052015
PheGenI	rs796052015
Biobank	rs796052015
1000 genomes	rs796052015
hgdp	rs796052015
ensembl	rs796052015
geneview	rs796052015
scholar	rs796052015
google	rs796052015
pharmgkb	rs796052015
gwascentral	rs796052015
openSNP	rs796052015
23andMe	rs796052015
SNPshot	rs796052015
SNPdbe	rs796052015
MSV3d	rs796052015
GWAS Ctlg	rs796052015

Max Magnitude

0

ClinVar
Risk	rs796052015(A;A)
Alt	rs796052015(A;A)
Reference	Rs796052015(-;-)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	OTC
CLNDBN	not provided
Reversed	0
HGVS	NC_000023.10:g.38229047dupA
CLNSRC
CLNACC	RCV000186070.1,