rs180177186

Orientation

plus

Stabilized

plus

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

Make rs180177186(A;G)

Make rs180177186(G;G)

Reference

GRCh38 38.1/141

Chromosome

2

Position

240869252

Gene

AGXT

is a	snp
is	mentioned by
dbSNP	rs180177186
dbSNP (classic)	rs180177186
ClinGen	rs180177186
ebi	rs180177186
HLI	rs180177186
Exac	rs180177186
Gnomad	rs180177186
Varsome	rs180177186
LitVar	rs180177186
Map	rs180177186
PheGenI	rs180177186
Biobank	rs180177186
1000 genomes	rs180177186
hgdp	rs180177186
ensembl	rs180177186
geneview	rs180177186
scholar	rs180177186
google	rs180177186
pharmgkb	rs180177186
gwascentral	rs180177186
openSNP	rs180177186
23andMe	rs180177186
SNPshot	rs180177186
SNPdbe	rs180177186
MSV3d	rs180177186
GWAS Ctlg	rs180177186

Max Magnitude

0

ClinVar
Risk	rs180177186(G;G)
Alt	rs180177186(G;G)
Reference	Rs180177186(A;A)
Significance	Pathogenic
Disease	Primary hyperoxaluria
Variation	info
Gene	AGXT
CLNDBN	Primary hyperoxaluria, type I
Reversed	0
HGVS	NC_000002.11:g.241808669A>G
CLNSRC
CLNACC	RCV000186291.1,