rs180177164

Orientation

plus

Stabilized

plus

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

Make rs180177164(-;-)

Make rs180177164(-;CG)

Reference

GRCh38 38.1/141

Chromosome

2

Position

240878767

Gene

AGXT

is a	snp
is	mentioned by
dbSNP	rs180177164
dbSNP (classic)	rs180177164
ClinGen	rs180177164
ebi	rs180177164
HLI	rs180177164
Exac	rs180177164
Gnomad	rs180177164
Varsome	rs180177164
LitVar	rs180177164
Map	rs180177164
PheGenI	rs180177164
Biobank	rs180177164
1000 genomes	rs180177164
hgdp	rs180177164
ensembl	rs180177164
geneview	rs180177164
scholar	rs180177164
google	rs180177164
pharmgkb	rs180177164
gwascentral	rs180177164
openSNP	rs180177164
23andMe	rs180177164
SNPshot	rs180177164
SNPdbe	rs180177164
MSV3d	rs180177164
GWAS Ctlg	rs180177164

Max Magnitude

0

ClinVar
Risk	rs180177164(-;-)
Alt	rs180177164(-;-)
Reference	Rs180177164(CG;CG)
Significance	Pathogenic
Disease	Primary hyperoxaluria
Variation	info
Gene	AGXT
CLNDBN	Primary hyperoxaluria, type I
Reversed	0
HGVS	NC_000002.11:g.241818184_241818185delCG
CLNSRC
CLNACC	RCV000186419.1,