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rs180177279

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs180177279(C;T)
Make rs180177279(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position240876002
GeneAGXT
is asnp
is mentioned by
dbSNPrs180177279
ebirs180177279
HLIrs180177279
Exacrs180177279
Varsomers180177279
Maprs180177279
PheGenIrs180177279
hapmaprs180177279
1000 genomesrs180177279
hgdprs180177279
ensemblrs180177279
gopubmedrs180177279
geneviewrs180177279
scholarrs180177279
googlers180177279
pharmgkbrs180177279
gwascentralrs180177279
openSNPrs180177279
23andMers180177279
23andMe allrs180177279
SNP Nexus

SNPshotrs180177279
SNPdbers180177279
MSV3drs180177279
GWAS Ctlgrs180177279
Max Magnitude0
ClinVar
Risk rs180177279(T;T)
Alt rs180177279(T;T)
Reference rs180177279(C;C)
Significance Pathogenic
Disease Primary hyperoxaluria
Variation info
Gene AGXT
CLNDBN Primary hyperoxaluria, type I
Reversed 0
HGVS NC_000002.11:g.241815419C>T
CLNSRC
CLNACC RCV000186337.1,