rs180177173

Orientation

plus

Stabilized

plus

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

Make rs180177173(A;A)

Make rs180177173(A;G)

Reference

GRCh38 38.1/141

Chromosome

2

Position

240869004

Gene

AGXT

is a	snp
is	mentioned by
dbSNP	rs180177173
dbSNP (classic)	rs180177173
ClinGen	rs180177173
ebi	rs180177173
HLI	rs180177173
Exac	rs180177173
Gnomad	rs180177173
Varsome	rs180177173
LitVar	rs180177173
Map	rs180177173
PheGenI	rs180177173
Biobank	rs180177173
1000 genomes	rs180177173
hgdp	rs180177173
ensembl	rs180177173
geneview	rs180177173
scholar	rs180177173
google	rs180177173
pharmgkb	rs180177173
gwascentral	rs180177173
openSNP	rs180177173
23andMe	rs180177173
SNPshot	rs180177173
SNPdbe	rs180177173
MSV3d	rs180177173
GWAS Ctlg	rs180177173

Max Magnitude

0

ClinVar
Risk	rs180177173(A;A) rs180177173(C;C)
Alt	rs180177173(A;A) rs180177173(C;C)
Reference	Rs180177173(G;G)
Significance	Pathogenic
Disease	Primary hyperoxaluria
Variation	info
Gene	AGXT
CLNDBN	Primary hyperoxaluria, type I
Reversed	0
HGVS	NC_000002.11:g.241808421G>A
CLNSRC	UniProtKB (protein)
CLNACC	RCV000186282.1,