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rs180177262

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs180177262(G;G)
Make rs180177262(G;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position240868939
GeneAGXT
is asnp
is mentioned by
dbSNPrs180177262
ebirs180177262
HLIrs180177262
Exacrs180177262
Varsomers180177262
Maprs180177262
PheGenIrs180177262
hapmaprs180177262
1000 genomesrs180177262
hgdprs180177262
ensemblrs180177262
gopubmedrs180177262
geneviewrs180177262
scholarrs180177262
googlers180177262
pharmgkbrs180177262
gwascentralrs180177262
openSNPrs180177262
23andMers180177262
23andMe allrs180177262
SNP Nexus

SNPshotrs180177262
SNPdbers180177262
MSV3drs180177262
GWAS Ctlgrs180177262
Max Magnitude0
ClinVar
Risk rs180177262(G;G)
Alt rs180177262(G;G)
Reference rs180177262(T;T)
Significance Pathogenic
Disease Primary hyperoxaluria
Variation info
Gene AGXT
CLNDBN Primary hyperoxaluria, type I
Reversed 0
HGVS NC_000002.11:g.241808356T>G
CLNSRC
CLNACC RCV000186276.1,