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rs180177197

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs180177197(C;C)
Make rs180177197(C;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position240869326
GeneAGXT
is asnp
is mentioned by
dbSNPrs180177197
ebirs180177197
HLIrs180177197
Exacrs180177197
Varsomers180177197
Maprs180177197
PheGenIrs180177197
hapmaprs180177197
1000 genomesrs180177197
hgdprs180177197
ensemblrs180177197
gopubmedrs180177197
geneviewrs180177197
scholarrs180177197
googlers180177197
pharmgkbrs180177197
gwascentralrs180177197
openSNPrs180177197
23andMers180177197
23andMe allrs180177197
SNP Nexus

SNPshotrs180177197
SNPdbers180177197
MSV3drs180177197
GWAS Ctlgrs180177197
Max Magnitude0
ClinVar
Risk rs180177197(C;C)
Alt rs180177197(C;C)
Reference rs180177197(T;T)
Significance Other
Disease Primary hyperoxaluria
Variation info
Gene AGXT
CLNDBN Primary hyperoxaluria, type I
Reversed 0
HGVS NC_000002.11:g.241808743T>C
CLNSRC
CLNACC RCV000169249.2,