rs1057516896

Orientation

plus

Stabilized

plus

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

Make rs1057516896(-;-)

Make rs1057516896(-;AAGG)

Reference

GRCh38.p7 38.3/150

Chromosome

2

Position

240874055

Gene

AGXT

is a	snp
is	mentioned by
dbSNP	rs1057516896
dbSNP (classic)	rs1057516896
ClinGen	rs1057516896
ebi	rs1057516896
HLI	rs1057516896
Exac	rs1057516896
Gnomad	rs1057516896
Varsome	rs1057516896
LitVar	rs1057516896
Map	rs1057516896
PheGenI	rs1057516896
Biobank	rs1057516896
1000 genomes	rs1057516896
hgdp	rs1057516896
ensembl	rs1057516896
geneview	rs1057516896
scholar	rs1057516896
google	rs1057516896
pharmgkb	rs1057516896
gwascentral	rs1057516896
openSNP	rs1057516896
23andMe	rs1057516896
SNPshot	rs1057516896
SNPdbe	rs1057516896
MSV3d	rs1057516896
GWAS Ctlg	rs1057516896

Max Magnitude

0

ClinVar
Risk	rs1057516896(-;-)
Alt	rs1057516896(-;-)
Reference	Rs1057516896(AAGG;AAGG)
Significance	Probable-Pathogenic
Disease	Primary hyperoxaluria
Variation	info
Gene	AGXT
CLNDBN	Primary hyperoxaluria, type I
Reversed	0
HGVS	NC_000002.11:g.241813472_241813475delAAGG
CLNSRC
CLNACC	RCV000410991.1,