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rs180177189

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs180177189(A;A)
Make rs180177189(A;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position240869287
GeneAGXT
is asnp
is mentioned by
dbSNPrs180177189
ebirs180177189
HLIrs180177189
Exacrs180177189
Varsomers180177189
Maprs180177189
PheGenIrs180177189
hapmaprs180177189
1000 genomesrs180177189
hgdprs180177189
ensemblrs180177189
gopubmedrs180177189
geneviewrs180177189
scholarrs180177189
googlers180177189
pharmgkbrs180177189
gwascentralrs180177189
openSNPrs180177189
23andMers180177189
23andMe allrs180177189
SNP Nexus

SNPshotrs180177189
SNPdbers180177189
MSV3drs180177189
GWAS Ctlgrs180177189
Max Magnitude0
ClinVar
Risk rs180177189(A;A)
Alt rs180177189(A;A)
Reference rs180177189(G;G)
Significance Pathogenic
Disease Primary hyperoxaluria
Variation info
Gene AGXT
CLNDBN Primary hyperoxaluria, type I
Reversed 0
HGVS NC_000002.11:g.241808704G>A
CLNSRC
CLNACC RCV000186293.1,