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rs180177285

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs180177285(C;C)
Make rs180177285(C;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position240877536
GeneAGXT
is asnp
is mentioned by
dbSNPrs180177285
ebirs180177285
HLIrs180177285
Exacrs180177285
Varsomers180177285
Maprs180177285
PheGenIrs180177285
hapmaprs180177285
1000 genomesrs180177285
hgdprs180177285
ensemblrs180177285
gopubmedrs180177285
geneviewrs180177285
scholarrs180177285
googlers180177285
pharmgkbrs180177285
gwascentralrs180177285
openSNPrs180177285
23andMers180177285
23andMe allrs180177285
SNP Nexus

SNPshotrs180177285
SNPdbers180177285
MSV3drs180177285
GWAS Ctlgrs180177285
Max Magnitude0
ClinVar
Risk rs180177285(C;C)
Alt rs180177285(C;C)
Reference rs180177285(G;G)
Significance Pathogenic
Disease Primary hyperoxaluria
Variation info
Gene AGXT
CLNDBN Primary hyperoxaluria, type I
Reversed 0
HGVS NC_000002.11:g.241816953G>C
CLNSRC
CLNACC RCV000186375.1,