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rs180177253

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs180177253(C;T)
Make rs180177253(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position240874035
GeneAGXT
is asnp
is mentioned by
dbSNPrs180177253
ebirs180177253
HLIrs180177253
Exacrs180177253
Varsomers180177253
Maprs180177253
PheGenIrs180177253
hapmaprs180177253
1000 genomesrs180177253
hgdprs180177253
ensemblrs180177253
gopubmedrs180177253
geneviewrs180177253
scholarrs180177253
googlers180177253
pharmgkbrs180177253
gwascentralrs180177253
openSNPrs180177253
23andMers180177253
23andMe allrs180177253
SNP Nexus

SNPshotrs180177253
SNPdbers180177253
MSV3drs180177253
GWAS Ctlgrs180177253
Max Magnitude0
ClinVar
Risk rs180177253(T;T)
Alt rs180177253(T;T)
Reference rs180177253(C;C)
Significance Other
Disease Primary hyperoxaluria
Variation info
Gene AGXT
CLNDBN Primary hyperoxaluria, type I
Reversed 0
HGVS NC_000002.11:g.241813452C>T
CLNSRC
CLNACC RCV000169358.2,