rs180177158

Orientation

plus

Stabilized

plus

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

Make rs180177158(A;A)

Make rs180177158(A;G)

Reference

GRCh38 38.1/141

Chromosome

2

Position

240878151

Gene

AGXT

is a	snp
is	mentioned by
dbSNP	rs180177158
dbSNP (classic)	rs180177158
ClinGen	rs180177158
ebi	rs180177158
HLI	rs180177158
Exac	rs180177158
Gnomad	rs180177158
Varsome	rs180177158
LitVar	rs180177158
Map	rs180177158
PheGenI	rs180177158
Biobank	rs180177158
1000 genomes	rs180177158
hgdp	rs180177158
ensembl	rs180177158
geneview	rs180177158
scholar	rs180177158
google	rs180177158
pharmgkb	rs180177158
gwascentral	rs180177158
openSNP	rs180177158
23andMe	rs180177158
SNPshot	rs180177158
SNPdbe	rs180177158
MSV3d	rs180177158
GWAS Ctlg	rs180177158

Max Magnitude

0

ClinVar
Risk	rs180177158(A;A)
Alt	rs180177158(A;A)
Reference	Rs180177158(G;G)
Significance	Pathogenic
Disease	Primary hyperoxaluria
Variation	info
Gene	AGXT
CLNDBN	Primary hyperoxaluria, type I
Reversed	0
HGVS	NC_000002.11:g.241817568G>A
CLNSRC
CLNACC	RCV000186369.1,