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rs180177277

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs180177277(G;G)
Make rs180177277(G;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position240875995
GeneAGXT
is asnp
is mentioned by
dbSNPrs180177277
ebirs180177277
HLIrs180177277
Exacrs180177277
Varsomers180177277
Maprs180177277
PheGenIrs180177277
hapmaprs180177277
1000 genomesrs180177277
hgdprs180177277
ensemblrs180177277
gopubmedrs180177277
geneviewrs180177277
scholarrs180177277
googlers180177277
pharmgkbrs180177277
gwascentralrs180177277
openSNPrs180177277
23andMers180177277
23andMe allrs180177277
SNP Nexus

SNPshotrs180177277
SNPdbers180177277
MSV3drs180177277
GWAS Ctlgrs180177277
Max Magnitude0
ClinVar
Risk rs180177277(G;G)
Alt rs180177277(G;G)
Reference rs180177277(T;T)
Significance Pathogenic
Disease Primary hyperoxaluria
Variation info
Gene AGXT
CLNDBN Primary hyperoxaluria, type I
Reversed 0
HGVS NC_000002.11:g.241815412T>G
CLNSRC
CLNACC RCV000186257.1,