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rs111742810

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs111742810(A;A)
Make rs111742810(A;T)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position240874064
GeneAGXT
is asnp
is mentioned by
dbSNPrs111742810
ebirs111742810
HLIrs111742810
Exacrs111742810
Varsomers111742810
Maprs111742810
PheGenIrs111742810
hapmaprs111742810
1000 genomesrs111742810
hgdprs111742810
ensemblrs111742810
gopubmedrs111742810
geneviewrs111742810
scholarrs111742810
googlers111742810
pharmgkbrs111742810
gwascentralrs111742810
openSNPrs111742810
23andMers111742810
23andMe allrs111742810
SNP Nexus

SNPshotrs111742810
SNPdbers111742810
MSV3drs111742810
GWAS Ctlgrs111742810
Max Magnitude0
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,