rs121908524

Orientation

plus

Stabilized

plus

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

Make rs121908524(A;A)

Make rs121908524(A;T)

Reference

GRCh38 38.1/141

Chromosome

2

Position

240871379

Gene

AGXT

is a	snp
is	mentioned by
dbSNP	rs121908524
dbSNP (classic)	rs121908524
ClinGen	rs121908524
ebi	rs121908524
HLI	rs121908524
Exac	rs121908524
Gnomad	rs121908524
Varsome	rs121908524
LitVar	rs121908524
Map	rs121908524
PheGenI	rs121908524
Biobank	rs121908524
1000 genomes	rs121908524
hgdp	rs121908524
ensembl	rs121908524
geneview	rs121908524
scholar	rs121908524
google	rs121908524
pharmgkb	rs121908524
gwascentral	rs121908524
openSNP	rs121908524
23andMe	rs121908524
SNPshot	rs121908524
SNPdbe	rs121908524
MSV3d	rs121908524
GWAS Ctlg	rs121908524

Max Magnitude

0

OMIM	604285
Desc
Variant	0006
Related	also

ClinVar
Risk	rs121908524(A;A)
Alt	rs121908524(A;A)
Reference	Rs121908524(T;T)
Significance	Pathogenic
Disease	Primary hyperoxaluria
Variation	info
Gene	AGXT
CLNDBN	Primary hyperoxaluria, type I
Reversed	0
HGVS	NC_000002.11:g.241810796T>A
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000005999.5,