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rs180177296

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs180177296(C;T)
Make rs180177296(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position240877612
GeneAGXT
is asnp
is mentioned by
dbSNPrs180177296
ebirs180177296
HLIrs180177296
Exacrs180177296
Varsomers180177296
Maprs180177296
PheGenIrs180177296
hapmaprs180177296
1000 genomesrs180177296
hgdprs180177296
ensemblrs180177296
gopubmedrs180177296
geneviewrs180177296
scholarrs180177296
googlers180177296
pharmgkbrs180177296
gwascentralrs180177296
openSNPrs180177296
23andMers180177296
23andMe allrs180177296
SNP Nexus

SNPshotrs180177296
SNPdbers180177296
MSV3drs180177296
GWAS Ctlgrs180177296
Max Magnitude0
ClinVar
Risk rs180177296(T;T)
Alt rs180177296(T;T)
Reference rs180177296(C;C)
Significance Pathogenic
Disease Primary hyperoxaluria
Variation info
Gene AGXT
CLNDBN Primary hyperoxaluria, type I
Reversed 0
HGVS NC_000002.11:g.241817029C>T
CLNSRC
CLNACC RCV000186345.1,