rs180177161

Orientation

plus

Stabilized

plus

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

Make rs180177161(A;A)

Make rs180177161(A;G)

Reference

GRCh38 38.1/141

Chromosome

2

Position

240878721

Gene

AGXT

is a	snp
is	mentioned by
dbSNP	rs180177161
dbSNP (classic)	rs180177161
ClinGen	rs180177161
ebi	rs180177161
HLI	rs180177161
Exac	rs180177161
Gnomad	rs180177161
Varsome	rs180177161
LitVar	rs180177161
Map	rs180177161
PheGenI	rs180177161
Biobank	rs180177161
1000 genomes	rs180177161
hgdp	rs180177161
ensembl	rs180177161
geneview	rs180177161
scholar	rs180177161
google	rs180177161
pharmgkb	rs180177161
gwascentral	rs180177161
openSNP	rs180177161
23andMe	rs180177161
SNPshot	rs180177161
SNPdbe	rs180177161
MSV3d	rs180177161
GWAS Ctlg	rs180177161

Max Magnitude

0

ClinVar
Risk	rs180177161(A;A)
Alt	rs180177161(A;A)
Reference	Rs180177161(G;G)
Significance	Pathogenic
Disease	Primary hyperoxaluria
Variation	info
Gene	AGXT
CLNDBN	Primary hyperoxaluria, type I
Reversed	0
HGVS	NC_000002.11:g.241818138G>A
CLNSRC
CLNACC	RCV000186354.1,