rs180177171

Orientation

plus

Stabilized

plus

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

Make rs180177171(-;-)

Make rs180177171(-;G)

Reference

GRCh38 38.1/141

Chromosome

2

Position

240868991

Gene

AGXT

is a	snp
is	mentioned by
dbSNP	rs180177171
dbSNP (classic)	rs180177171
ClinGen	rs180177171
ebi	rs180177171
HLI	rs180177171
Exac	rs180177171
Gnomad	rs180177171
Varsome	rs180177171
LitVar	rs180177171
Map	rs180177171
PheGenI	rs180177171
Biobank	rs180177171
1000 genomes	rs180177171
hgdp	rs180177171
ensembl	rs180177171
geneview	rs180177171
scholar	rs180177171
google	rs180177171
pharmgkb	rs180177171
gwascentral	rs180177171
openSNP	rs180177171
23andMe	rs180177171
SNPshot	rs180177171
SNPdbe	rs180177171
MSV3d	rs180177171
GWAS Ctlg	rs180177171

Max Magnitude

0

ClinVar
Risk	rs180177171(-;-)
Alt	rs180177171(-;-)
Reference	Rs180177171(G;G)
Significance	Pathogenic
Disease	Primary hyperoxaluria
Variation	info
Gene	AGXT
CLNDBN	Primary hyperoxaluria, type I
Reversed	0
HGVS	NC_000002.11:g.241808408delG
CLNSRC
CLNACC	RCV000186383.1,