rs796052074

Orientation

plus

Stabilized

plus

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

Make rs796052074(-;-)

Make rs796052074(-;CA)

Reference

GRCh38.p2 38.2/146

Chromosome

2

Position

240878038

Gene

AGXT

is a	snp
is	mentioned by
dbSNP	rs796052074
dbSNP (classic)	rs796052074
ClinGen	rs796052074
ebi	rs796052074
HLI	rs796052074
Exac	rs796052074
Gnomad	rs796052074
Varsome	rs796052074
LitVar	rs796052074
Map	rs796052074
PheGenI	rs796052074
Biobank	rs796052074
1000 genomes	rs796052074
hgdp	rs796052074
ensembl	rs796052074
geneview	rs796052074
scholar	rs796052074
google	rs796052074
pharmgkb	rs796052074
gwascentral	rs796052074
openSNP	rs796052074
23andMe	rs796052074
SNPshot	rs796052074
SNPdbe	rs796052074
MSV3d	rs796052074
GWAS Ctlg	rs796052074

Max Magnitude

0

ClinVar
Risk	rs796052074(-;-)
Alt	rs796052074(-;-)
Reference	Rs796052074(CA;CA)
Significance	Pathogenic
Disease	Primary hyperoxaluria
Variation	info
Gene	AGXT
CLNDBN	Primary hyperoxaluria, type I
Reversed	0
HGVS	NC_000002.11:g.241817455_241817456delCA
CLNSRC
CLNACC	RCV000186415.1,