rs180177162

Orientation

plus

Stabilized

plus

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

Make rs180177162(A;A)

Make rs180177162(A;G)

Reference

GRCh38 38.1/141

Chromosome

2

Position

240868972

Gene

AGXT

is a	snp
is	mentioned by
dbSNP	rs180177162
dbSNP (classic)	rs180177162
ClinGen	rs180177162
ebi	rs180177162
HLI	rs180177162
Exac	rs180177162
Gnomad	rs180177162
Varsome	rs180177162
LitVar	rs180177162
Map	rs180177162
PheGenI	rs180177162
Biobank	rs180177162
1000 genomes	rs180177162
hgdp	rs180177162
ensembl	rs180177162
geneview	rs180177162
scholar	rs180177162
google	rs180177162
pharmgkb	rs180177162
gwascentral	rs180177162
openSNP	rs180177162
23andMe	rs180177162
SNPshot	rs180177162
SNPdbe	rs180177162
MSV3d	rs180177162
GWAS Ctlg	rs180177162

Max Magnitude

0

ClinVar
Risk	rs180177162(A;A)
Alt	rs180177162(A;A)
Reference	Rs180177162(G;G)
Significance	Pathogenic
Disease	Primary hyperoxaluria
Variation	info
Gene	AGXT
CLNDBN	Primary hyperoxaluria, type I
Reversed	0
HGVS	NC_000002.11:g.241808389G>A
CLNSRC
CLNACC	RCV000186278.1,