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rs138025751

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs138025751(C;C)
Make rs138025751(C;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position240869357
GeneAGXT
is asnp
is mentioned by
dbSNPrs138025751
ebirs138025751
HLIrs138025751
Exacrs138025751
Varsomers138025751
Maprs138025751
PheGenIrs138025751
hapmaprs138025751
1000 genomesrs138025751
hgdprs138025751
ensemblrs138025751
gopubmedrs138025751
geneviewrs138025751
scholarrs138025751
googlers138025751
pharmgkbrs138025751
gwascentralrs138025751
openSNPrs138025751
23andMers138025751
23andMe allrs138025751
SNP Nexus

SNPshotrs138025751
SNPdbers138025751
MSV3drs138025751
GWAS Ctlgrs138025751
Max Magnitude0
ClinVar
Risk rs138025751(A,C;A,C)
Alt rs138025751(A,C;A,C)
Reference rs138025751(G;G)
Significance Pathogenic
Disease Primary hyperoxaluria
Variation info
Gene AGXT
CLNDBN Primary hyperoxaluria, type I
Reversed 0
HGVS NC_000002.11:g.241808774G>A
CLNSRC
CLNACC RCV000186302.1,