rs180177240

Orientation

plus

Stabilized

plus

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

Make rs180177240(-;-)

Make rs180177240(-;G)

Reference

GRCh38 38.1/141

Chromosome

2

Position

240873024

Gene

AGXT

is a	snp
is	mentioned by
dbSNP	rs180177240
dbSNP (classic)	rs180177240
ClinGen	rs180177240
ebi	rs180177240
HLI	rs180177240
Exac	rs180177240
Gnomad	rs180177240
Varsome	rs180177240
LitVar	rs180177240
Map	rs180177240
PheGenI	rs180177240
Biobank	rs180177240
1000 genomes	rs180177240
hgdp	rs180177240
ensembl	rs180177240
geneview	rs180177240
scholar	rs180177240
google	rs180177240
pharmgkb	rs180177240
gwascentral	rs180177240
openSNP	rs180177240
23andMe	rs180177240
SNPshot	rs180177240
SNPdbe	rs180177240
MSV3d	rs180177240
GWAS Ctlg	rs180177240

Max Magnitude

0

ClinVar
Risk	rs180177240(-;-)
Alt	rs180177240(-;-)
Reference	Rs180177240(G;G)
Significance	Pathogenic
Disease	Primary hyperoxaluria
Variation	info
Gene	AGXT
CLNDBN	Primary hyperoxaluria, type I
Reversed	0
HGVS	NC_000002.11:g.241812441delG
CLNSRC
CLNACC	RCV000186397.1,