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rs121908525

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs121908525(C;C)
Make rs121908525(C;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position240875159
GeneAGXT
is asnp
is mentioned by
dbSNPrs121908525
ebirs121908525
HLIrs121908525
Exacrs121908525
Varsomers121908525
Maprs121908525
PheGenIrs121908525
hapmaprs121908525
1000 genomesrs121908525
hgdprs121908525
ensemblrs121908525
gopubmedrs121908525
geneviewrs121908525
scholarrs121908525
googlers121908525
pharmgkbrs121908525
gwascentralrs121908525
openSNPrs121908525
23andMers121908525
23andMe allrs121908525
SNP Nexus

SNPshotrs121908525
SNPdbers121908525
MSV3drs121908525
GWAS Ctlgrs121908525
Max Magnitude0
OMIM604285
Desc
Variant0007
Relatedalso
ClinVar
Risk rs121908525(C;C)
Alt rs121908525(C;C)
Reference rs121908525(T;T)
Significance Pathogenic
Disease Primary hyperoxaluria
Variation info
Gene AGXT
CLNDBN Primary hyperoxaluria, type I
Reversed 0
HGVS NC_000002.11:g.241814576T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000006000.4,