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rs180177256

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs180177256(C;C)
Make rs180177256(C;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position240874067
GeneAGXT
is asnp
is mentioned by
dbSNPrs180177256
ebirs180177256
HLIrs180177256
Exacrs180177256
Varsomers180177256
Maprs180177256
PheGenIrs180177256
hapmaprs180177256
1000 genomesrs180177256
hgdprs180177256
ensemblrs180177256
gopubmedrs180177256
geneviewrs180177256
scholarrs180177256
googlers180177256
pharmgkbrs180177256
gwascentralrs180177256
openSNPrs180177256
23andMers180177256
23andMe allrs180177256
SNP Nexus

SNPshotrs180177256
SNPdbers180177256
MSV3drs180177256
GWAS Ctlgrs180177256
Max Magnitude0
ClinVar
Risk rs180177256(C;C)
Alt rs180177256(C;C)
Reference rs180177256(G;G)
Significance Pathogenic
Disease Primary hyperoxaluria
Variation info
Gene AGXT
CLNDBN Primary hyperoxaluria, type I
Reversed 0
HGVS NC_000002.11:g.241813484G>C
CLNSRC
CLNACC RCV000186363.1,