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rs138584408

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs138584408(C;C)
Make rs138584408(C;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position240868867
GeneAGXT
is asnp
is mentioned by
dbSNPrs138584408
ebirs138584408
HLIrs138584408
Exacrs138584408
Varsomers138584408
Maprs138584408
PheGenIrs138584408
hapmaprs138584408
1000 genomesrs138584408
hgdprs138584408
ensemblrs138584408
gopubmedrs138584408
geneviewrs138584408
scholarrs138584408
googlers138584408
pharmgkbrs138584408
gwascentralrs138584408
openSNPrs138584408
23andMers138584408
23andMe allrs138584408
SNP Nexus

SNPshotrs138584408
SNPdbers138584408
MSV3drs138584408
GWAS Ctlgrs138584408
Max Magnitude0
ClinVar
Risk rs138584408(C;C)
Alt rs138584408(C;C)
Reference rs138584408(T;T)
Significance Pathogenic
Disease Primary hyperoxaluria
Variation info
Gene AGXT
CLNDBN Primary hyperoxaluria, type I
Reversed 0
HGVS NC_000002.11:g.241808284T>C
CLNSRC
CLNACC RCV000186271.1,