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rs180177155

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs180177155(A;A)
Make rs180177155(A;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position240878086
GeneAGXT
is asnp
is mentioned by
dbSNPrs180177155
ebirs180177155
HLIrs180177155
Exacrs180177155
Varsomers180177155
Maprs180177155
PheGenIrs180177155
hapmaprs180177155
1000 genomesrs180177155
hgdprs180177155
ensemblrs180177155
gopubmedrs180177155
geneviewrs180177155
scholarrs180177155
googlers180177155
pharmgkbrs180177155
gwascentralrs180177155
openSNPrs180177155
23andMers180177155
23andMe allrs180177155
SNP Nexus

SNPshotrs180177155
SNPdbers180177155
MSV3drs180177155
GWAS Ctlgrs180177155
Max Magnitude0
ClinVar
Risk rs180177155(A;A)
Alt rs180177155(A;A)
Reference Rs180177155(T;T)
Significance Pathogenic
Disease Primary hyperoxaluria
Variation info
Gene AGXT
CLNDBN Primary hyperoxaluria, type I
Reversed 0
HGVS NC_000002.11:g.241817503T>A
CLNSRC UniProtKB (protein)
CLNACC RCV000186350.1,