rs180177155

Orientation

plus

Stabilized

plus

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

Make rs180177155(A;A)

Make rs180177155(A;T)

Reference

GRCh38 38.1/141

Chromosome

2

Position

240878086

Gene

AGXT

is a	snp
is	mentioned by
dbSNP	rs180177155
dbSNP (classic)	rs180177155
ClinGen	rs180177155
ebi	rs180177155
HLI	rs180177155
Exac	rs180177155
Gnomad	rs180177155
Varsome	rs180177155
LitVar	rs180177155
Map	rs180177155
PheGenI	rs180177155
Biobank	rs180177155
1000 genomes	rs180177155
hgdp	rs180177155
ensembl	rs180177155
geneview	rs180177155
scholar	rs180177155
google	rs180177155
pharmgkb	rs180177155
gwascentral	rs180177155
openSNP	rs180177155
23andMe	rs180177155
SNPshot	rs180177155
SNPdbe	rs180177155
MSV3d	rs180177155
GWAS Ctlg	rs180177155

Max Magnitude

0

ClinVar
Risk	rs180177155(A;A)
Alt	rs180177155(A;A)
Reference	Rs180177155(T;T)
Significance	Pathogenic
Disease	Primary hyperoxaluria
Variation	info
Gene	AGXT
CLNDBN	Primary hyperoxaluria, type I
Reversed	0
HGVS	NC_000002.11:g.241817503T>A
CLNSRC	UniProtKB (protein)
CLNACC	RCV000186350.1,