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rs180177292

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs180177292(G;G)
Make rs180177292(G;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position240877581
GeneAGXT
is asnp
is mentioned by
dbSNPrs180177292
ebirs180177292
HLIrs180177292
Exacrs180177292
Varsomers180177292
Maprs180177292
PheGenIrs180177292
hapmaprs180177292
1000 genomesrs180177292
hgdprs180177292
ensemblrs180177292
gopubmedrs180177292
geneviewrs180177292
scholarrs180177292
googlers180177292
pharmgkbrs180177292
gwascentralrs180177292
openSNPrs180177292
23andMers180177292
23andMe allrs180177292
SNP Nexus

SNPshotrs180177292
SNPdbers180177292
MSV3drs180177292
GWAS Ctlgrs180177292
Max Magnitude0
ClinVar
Risk rs180177292(G;G)
Alt rs180177292(G;G)
Reference rs180177292(T;T)
Significance Pathogenic
Disease Primary hyperoxaluria
Variation info
Gene AGXT
CLNDBN Primary hyperoxaluria, type I
Reversed 0
HGVS NC_000002.11:g.241816998T>G
CLNSRC
CLNACC RCV000186342.1,