rs180177201

Orientation

plus

Stabilized

plus

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

Make rs180177201(-;-)

Make rs180177201(-;CC)

Reference

GRCh38 38.1/141

Chromosome

2

Position

240868897

Gene

AGXT

is a	snp
is	mentioned by
dbSNP	rs180177201
dbSNP (classic)	rs180177201
ClinGen	rs180177201
ebi	rs180177201
HLI	rs180177201
Exac	rs180177201
Gnomad	rs180177201
Varsome	rs180177201
LitVar	rs180177201
Map	rs180177201
PheGenI	rs180177201
Biobank	rs180177201
1000 genomes	rs180177201
hgdp	rs180177201
ensembl	rs180177201
geneview	rs180177201
scholar	rs180177201
google	rs180177201
pharmgkb	rs180177201
gwascentral	rs180177201
openSNP	rs180177201
23andMe	rs180177201
SNPshot	rs180177201
SNPdbe	rs180177201
MSV3d	rs180177201
GWAS Ctlg	rs180177201

Max Magnitude

0

ClinVar
Risk	rs180177201(-;-)
Alt	rs180177201(-;-)
Reference	Rs180177201(CC;CC)
Significance	Pathogenic
Disease	Primary hyperoxaluria
Variation	info
Gene	AGXT
CLNDBN	Primary hyperoxaluria, type I
Reversed	0
HGVS	NC_000002.11:g.241808314_241808315delCC
CLNSRC
CLNACC	RCV000186380.1,