rs180177177

Orientation

plus

Stabilized

plus

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

Make rs180177177(A;A)

Make rs180177177(A;G)

Reference

GRCh38 38.1/141

Chromosome

2

Position

240869169

Gene

AGXT

is a	snp
is	mentioned by
dbSNP	rs180177177
dbSNP (classic)	rs180177177
ClinGen	rs180177177
ebi	rs180177177
HLI	rs180177177
Exac	rs180177177
Gnomad	rs180177177
Varsome	rs180177177
LitVar	rs180177177
Map	rs180177177
PheGenI	rs180177177
Biobank	rs180177177
1000 genomes	rs180177177
hgdp	rs180177177
ensembl	rs180177177
geneview	rs180177177
scholar	rs180177177
google	rs180177177
pharmgkb	rs180177177
gwascentral	rs180177177
openSNP	rs180177177
23andMe	rs180177177
SNPshot	rs180177177
SNPdbe	rs180177177
MSV3d	rs180177177
GWAS Ctlg	rs180177177

Max Magnitude

0

ClinVar
Risk	rs180177177(A;A)
Alt	rs180177177(A;A)
Reference	Rs180177177(G;G)
Significance	Pathogenic
Disease	Primary hyperoxaluria
Variation	info
Gene	AGXT
CLNDBN	Primary hyperoxaluria, type I
Reversed	0
HGVS	NC_000002.11:g.241808586G>A
CLNSRC
CLNACC	RCV000186370.1,