rs180177189

Orientation

plus

Stabilized

plus

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

Make rs180177189(A;A)

Make rs180177189(A;G)

Reference

GRCh38 38.1/141

Chromosome

2

Position

240869287

Gene

AGXT

is a	snp
is	mentioned by
dbSNP	rs180177189
dbSNP (classic)	rs180177189
ClinGen	rs180177189
ebi	rs180177189
HLI	rs180177189
Exac	rs180177189
Gnomad	rs180177189
Varsome	rs180177189
LitVar	rs180177189
Map	rs180177189
PheGenI	rs180177189
Biobank	rs180177189
1000 genomes	rs180177189
hgdp	rs180177189
ensembl	rs180177189
geneview	rs180177189
scholar	rs180177189
google	rs180177189
pharmgkb	rs180177189
gwascentral	rs180177189
openSNP	rs180177189
23andMe	rs180177189
SNPshot	rs180177189
SNPdbe	rs180177189
MSV3d	rs180177189
GWAS Ctlg	rs180177189

Max Magnitude

0

ClinVar
Risk	rs180177189(A;A)
Alt	rs180177189(A;A)
Reference	Rs180177189(G;G)
Significance	Pathogenic
Disease	Primary hyperoxaluria
Variation	info
Gene	AGXT
CLNDBN	Primary hyperoxaluria, type I
Reversed	0
HGVS	NC_000002.11:g.241808704G>A
CLNSRC
CLNACC	RCV000186293.1,