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rs180177177

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs180177177(A;A)
Make rs180177177(A;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position240869169
GeneAGXT
is asnp
is mentioned by
dbSNPrs180177177
ebirs180177177
HLIrs180177177
Exacrs180177177
Varsomers180177177
Maprs180177177
PheGenIrs180177177
hapmaprs180177177
1000 genomesrs180177177
hgdprs180177177
ensemblrs180177177
gopubmedrs180177177
geneviewrs180177177
scholarrs180177177
googlers180177177
pharmgkbrs180177177
gwascentralrs180177177
openSNPrs180177177
23andMers180177177
23andMe allrs180177177
SNP Nexus

SNPshotrs180177177
SNPdbers180177177
MSV3drs180177177
GWAS Ctlgrs180177177
Max Magnitude0
ClinVar
Risk rs180177177(A;A)
Alt rs180177177(A;A)
Reference rs180177177(G;G)
Significance Pathogenic
Disease Primary hyperoxaluria
Variation info
Gene AGXT
CLNDBN Primary hyperoxaluria, type I
Reversed 0
HGVS NC_000002.11:g.241808586G>A
CLNSRC
CLNACC RCV000186370.1,