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rs180177280

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs180177280(A;G)
Make rs180177280(G;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position240876003
GeneAGXT
is asnp
is mentioned by
dbSNPrs180177280
ebirs180177280
HLIrs180177280
Exacrs180177280
Varsomers180177280
Maprs180177280
PheGenIrs180177280
hapmaprs180177280
1000 genomesrs180177280
hgdprs180177280
ensemblrs180177280
gopubmedrs180177280
geneviewrs180177280
scholarrs180177280
googlers180177280
pharmgkbrs180177280
gwascentralrs180177280
openSNPrs180177280
23andMers180177280
23andMe allrs180177280
SNP Nexus

SNPshotrs180177280
SNPdbers180177280
MSV3drs180177280
GWAS Ctlgrs180177280
Max Magnitude0
ClinVar
Risk rs180177280(G;G)
Alt rs180177280(G;G)
Reference rs180177280(A;A)
Significance Pathogenic
Disease Primary hyperoxaluria
Variation info
Gene AGXT
CLNDBN Primary hyperoxaluria, type I
Reversed 0
HGVS NC_000002.11:g.241815420A>G
CLNSRC
CLNACC RCV000186259.1,