rs180177170

Orientation

plus

Stabilized

plus

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

Make rs180177170(A;A)

Make rs180177170(A;G)

Reference

GRCh38 38.1/141

Chromosome

2

Position

240868990

Gene

AGXT

is a	snp
is	mentioned by
dbSNP	rs180177170
dbSNP (classic)	rs180177170
ClinGen	rs180177170
ebi	rs180177170
HLI	rs180177170
Exac	rs180177170
Gnomad	rs180177170
Varsome	rs180177170
LitVar	rs180177170
Map	rs180177170
PheGenI	rs180177170
Biobank	rs180177170
1000 genomes	rs180177170
hgdp	rs180177170
ensembl	rs180177170
geneview	rs180177170
scholar	rs180177170
google	rs180177170
pharmgkb	rs180177170
gwascentral	rs180177170
openSNP	rs180177170
23andMe	rs180177170
SNPshot	rs180177170
SNPdbe	rs180177170
MSV3d	rs180177170
GWAS Ctlg	rs180177170

Max Magnitude

0

ClinVar
Risk	rs180177170(A;A)
Alt	rs180177170(A;A)
Reference	Rs180177170(G;G)
Significance	Pathogenic
Disease	Primary hyperoxaluria
Variation	info
Gene	AGXT
CLNDBN	Primary hyperoxaluria, type I
Reversed	0
HGVS	NC_000002.11:g.241808407G>A
CLNSRC
CLNACC	RCV000186280.1,