rs111742810

Orientation

plus

Stabilized

plus

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

Make rs111742810(A;A)

Make rs111742810(A;T)

Reference

GRCh38.p2 38.2/144

Chromosome

2

Position

240874064

Gene

AGXT

is a	snp
is	mentioned by
dbSNP	rs111742810
dbSNP (classic)	rs111742810
ClinGen	rs111742810
ebi	rs111742810
HLI	rs111742810
Exac	rs111742810
Gnomad	rs111742810
Varsome	rs111742810
LitVar	rs111742810
Map	rs111742810
PheGenI	rs111742810
Biobank	rs111742810
1000 genomes	rs111742810
hgdp	rs111742810
ensembl	rs111742810
geneview	rs111742810
scholar	rs111742810
google	rs111742810
pharmgkb	rs111742810
gwascentral	rs111742810
openSNP	rs111742810
23andMe	rs111742810
SNPshot	rs111742810
SNPdbe	rs111742810
MSV3d	rs111742810
GWAS Ctlg	rs111742810

Max Magnitude

0

ClinVar
Risk	rs111742810(A;A)
Alt	rs111742810(A;A)
Reference	Rs111742810(T;T)
Significance	Pathogenic
Disease	Primary hyperoxaluria
Variation	info
Gene	AGXT
CLNDBN	Primary hyperoxaluria, type I
Reversed	0
HGVS	NC_000002.11:g.241813481T>A
CLNSRC
CLNACC	RCV000186362.1,