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rs180177263

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs180177263(A;A)
Make rs180177263(A;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position240875181
GeneAGXT
is asnp
is mentioned by
dbSNPrs180177263
ebirs180177263
HLIrs180177263
Exacrs180177263
Varsomers180177263
Maprs180177263
PheGenIrs180177263
hapmaprs180177263
1000 genomesrs180177263
hgdprs180177263
ensemblrs180177263
gopubmedrs180177263
geneviewrs180177263
scholarrs180177263
googlers180177263
pharmgkbrs180177263
gwascentralrs180177263
openSNPrs180177263
23andMers180177263
23andMe allrs180177263
SNP Nexus

SNPshotrs180177263
SNPdbers180177263
MSV3drs180177263
GWAS Ctlgrs180177263
Max Magnitude0
ClinVar
Risk rs180177263(A;A)
Alt rs180177263(A;A)
Reference rs180177263(G;G)
Significance Pathogenic
Disease Primary hyperoxaluria
Variation info
Gene AGXT
CLNDBN Primary hyperoxaluria, type I
Reversed 0
HGVS NC_000002.11:g.241814598G>A
CLNSRC
CLNACC RCV000186331.1,