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rs180177267

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs180177267(C;C)
Make rs180177267(C;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position240875934
GeneAGXT
is asnp
is mentioned by
dbSNPrs180177267
ebirs180177267
HLIrs180177267
Exacrs180177267
Varsomers180177267
Maprs180177267
PheGenIrs180177267
hapmaprs180177267
1000 genomesrs180177267
hgdprs180177267
ensemblrs180177267
gopubmedrs180177267
geneviewrs180177267
scholarrs180177267
googlers180177267
pharmgkbrs180177267
gwascentralrs180177267
openSNPrs180177267
23andMers180177267
23andMe allrs180177267
SNP Nexus

SNPshotrs180177267
SNPdbers180177267
MSV3drs180177267
GWAS Ctlgrs180177267
Max Magnitude0
ClinVar
Risk rs180177267(C;C)
Alt rs180177267(C;C)
Reference rs180177267(G;G)
Significance Other
Disease Primary hyperoxaluria
Variation info
Gene AGXT
CLNDBN Primary hyperoxaluria, type I
Reversed 0
HGVS NC_000002.11:g.241815351G>C
CLNSRC
CLNACC RCV000169101.2,