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rs180177171

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs180177171(-;-)
Make rs180177171(-;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position240868991
GeneAGXT
is asnp
is mentioned by
dbSNPrs180177171
ebirs180177171
HLIrs180177171
Exacrs180177171
Varsomers180177171
Maprs180177171
PheGenIrs180177171
hapmaprs180177171
1000 genomesrs180177171
hgdprs180177171
ensemblrs180177171
gopubmedrs180177171
geneviewrs180177171
scholarrs180177171
googlers180177171
pharmgkbrs180177171
gwascentralrs180177171
openSNPrs180177171
23andMers180177171
23andMe allrs180177171
SNP Nexus

SNPshotrs180177171
SNPdbers180177171
MSV3drs180177171
GWAS Ctlgrs180177171
Max Magnitude0
ClinVar
Risk rs180177171(;)
Alt rs180177171(;)
Reference rs180177171(G;G)
Significance Pathogenic
Disease Primary hyperoxaluria
Variation info
Gene AGXT
CLNDBN Primary hyperoxaluria, type I
Reversed 0
HGVS NC_000002.11:g.241808408delG
CLNSRC
CLNACC RCV000186383.1,