rs180177163

Orientation

plus

Stabilized

plus

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

Make rs180177163(A;A)

Make rs180177163(A;G)

Reference

GRCh38.p2 38.2/144

Chromosome

2

Position

240878744

Gene

AGXT

is a	snp
is	mentioned by
dbSNP	rs180177163
dbSNP (classic)	rs180177163
ClinGen	rs180177163
ebi	rs180177163
HLI	rs180177163
Exac	rs180177163
Gnomad	rs180177163
Varsome	rs180177163
LitVar	rs180177163
Map	rs180177163
PheGenI	rs180177163
Biobank	rs180177163
1000 genomes	rs180177163
hgdp	rs180177163
ensembl	rs180177163
geneview	rs180177163
scholar	rs180177163
google	rs180177163
pharmgkb	rs180177163
gwascentral	rs180177163
openSNP	rs180177163
23andMe	rs180177163
SNPshot	rs180177163
SNPdbe	rs180177163
MSV3d	rs180177163
GWAS Ctlg	rs180177163

Max Magnitude

0

ClinVar
Risk	rs180177163(A;A)
Alt	rs180177163(A;A)
Reference	Rs180177163(G;G)
Significance	Pathogenic
Disease	Primary hyperoxaluria
Variation	info
Gene	AGXT
CLNDBN	Primary hyperoxaluria, type I
Reversed	0
HGVS	NC_000002.11:g.241818161G>A
CLNSRC
CLNACC	RCV000186355.1,