rs796052067

Orientation

plus

Stabilized

plus

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

Make rs796052067(G;T)

Make rs796052067(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

2

Position

240869363

Gene

AGXT

is a	snp
is	mentioned by
dbSNP	rs796052067
dbSNP (classic)	rs796052067
ClinGen	rs796052067
ebi	rs796052067
HLI	rs796052067
Exac	rs796052067
Gnomad	rs796052067
Varsome	rs796052067
LitVar	rs796052067
Map	rs796052067
PheGenI	rs796052067
Biobank	rs796052067
1000 genomes	rs796052067
hgdp	rs796052067
ensembl	rs796052067
geneview	rs796052067
scholar	rs796052067
google	rs796052067
pharmgkb	rs796052067
gwascentral	rs796052067
openSNP	rs796052067
23andMe	rs796052067
SNPshot	rs796052067
SNPdbe	rs796052067
MSV3d	rs796052067
GWAS Ctlg	rs796052067

Max Magnitude

0

ClinVar
Risk	rs796052067(T;T)
Alt	rs796052067(T;T)
Reference	Rs796052067(G;G)
Significance	Pathogenic
Disease	Primary hyperoxaluria
Variation	info
Gene	AGXT
CLNDBN	Primary hyperoxaluria, type I
Reversed	0
HGVS	NC_000002.11:g.241808780G>T
CLNSRC
CLNACC	RCV000186358.1,