rs180177279

Orientation

plus

Stabilized

plus

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

Make rs180177279(C;T)

Make rs180177279(T;T)

Reference

GRCh38 38.1/141

Chromosome

2

Position

240876002

Gene

AGXT

is a	snp
is	mentioned by
dbSNP	rs180177279
dbSNP (classic)	rs180177279
ClinGen	rs180177279
ebi	rs180177279
HLI	rs180177279
Exac	rs180177279
Gnomad	rs180177279
Varsome	rs180177279
LitVar	rs180177279
Map	rs180177279
PheGenI	rs180177279
Biobank	rs180177279
1000 genomes	rs180177279
hgdp	rs180177279
ensembl	rs180177279
geneview	rs180177279
scholar	rs180177279
google	rs180177279
pharmgkb	rs180177279
gwascentral	rs180177279
openSNP	rs180177279
23andMe	rs180177279
SNPshot	rs180177279
SNPdbe	rs180177279
MSV3d	rs180177279
GWAS Ctlg	rs180177279

Max Magnitude

0

ClinVar
Risk	rs180177279(A;A) rs180177279(T;T)
Alt	rs180177279(A;A) rs180177279(T;T)
Reference	Rs180177279(C;C)
Significance	Pathogenic
Disease	Primary hyperoxaluria
Variation	info
Gene	AGXT
CLNDBN	Primary hyperoxaluria, type I
Reversed	0
HGVS	NC_000002.11:g.241815419C>T
CLNSRC
CLNACC	RCV000186337.1,