rs796052062

Orientation

plus

Stabilized

plus

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

Make rs796052062(A;A)

Make rs796052062(A;G)

Reference

GRCh38.p2 38.2/146

Chromosome

2

Position

240873049

Gene

AGXT

is a	snp
is	mentioned by
dbSNP	rs796052062
dbSNP (classic)	rs796052062
ClinGen	rs796052062
ebi	rs796052062
HLI	rs796052062
Exac	rs796052062
Gnomad	rs796052062
Varsome	rs796052062
LitVar	rs796052062
Map	rs796052062
PheGenI	rs796052062
Biobank	rs796052062
1000 genomes	rs796052062
hgdp	rs796052062
ensembl	rs796052062
geneview	rs796052062
scholar	rs796052062
google	rs796052062
pharmgkb	rs796052062
gwascentral	rs796052062
openSNP	rs796052062
23andMe	rs796052062
SNPshot	rs796052062
SNPdbe	rs796052062
MSV3d	rs796052062
GWAS Ctlg	rs796052062

Max Magnitude

0

ClinVar
Risk	rs796052062(A;A)
Alt	rs796052062(A;A)
Reference	Rs796052062(G;G)
Significance	Pathogenic
Disease	Primary hyperoxaluria
Variation	info
Gene	AGXT
CLNDBN	Primary hyperoxaluria, type I
Reversed	0
HGVS	NC_000002.11:g.241812466G>A
CLNSRC
CLNACC	RCV000186320.1,