rs180177301

Orientation

plus

Stabilized

plus

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

Make rs180177301(-;-)

Make rs180177301(-;G)

Reference

GRCh38 38.1/141

Chromosome

2

Position

240878055

Gene

AGXT

is a	snp
is	mentioned by
dbSNP	rs180177301
dbSNP (classic)	rs180177301
ClinGen	rs180177301
ebi	rs180177301
HLI	rs180177301
Exac	rs180177301
Gnomad	rs180177301
Varsome	rs180177301
LitVar	rs180177301
Map	rs180177301
PheGenI	rs180177301
Biobank	rs180177301
1000 genomes	rs180177301
hgdp	rs180177301
ensembl	rs180177301
geneview	rs180177301
scholar	rs180177301
google	rs180177301
pharmgkb	rs180177301
gwascentral	rs180177301
openSNP	rs180177301
23andMe	rs180177301
SNPshot	rs180177301
SNPdbe	rs180177301
MSV3d	rs180177301
GWAS Ctlg	rs180177301

Max Magnitude

0

ClinVar
Risk	rs180177301(-;-)
Alt	rs180177301(-;-)
Reference	Rs180177301(G;G)
Significance	Other
Disease	Primary hyperoxaluria
Variation	info
Gene	AGXT
CLNDBN	Primary hyperoxaluria, type I
Reversed	0
HGVS	NC_000002.11:g.241817472delG
CLNSRC
CLNACC	RCV000169587.2,