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rs180177161

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs180177161(A;A)
Make rs180177161(A;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position240878721
GeneAGXT
is asnp
is mentioned by
dbSNPrs180177161
ebirs180177161
HLIrs180177161
Exacrs180177161
Varsomers180177161
Maprs180177161
PheGenIrs180177161
hapmaprs180177161
1000 genomesrs180177161
hgdprs180177161
ensemblrs180177161
gopubmedrs180177161
geneviewrs180177161
scholarrs180177161
googlers180177161
pharmgkbrs180177161
gwascentralrs180177161
openSNPrs180177161
23andMers180177161
23andMe allrs180177161
SNP Nexus

SNPshotrs180177161
SNPdbers180177161
MSV3drs180177161
GWAS Ctlgrs180177161
Max Magnitude0
ClinVar
Risk rs180177161(A;A)
Alt rs180177161(A;A)
Reference rs180177161(G;G)
Significance Pathogenic
Disease Primary hyperoxaluria
Variation info
Gene AGXT
CLNDBN Primary hyperoxaluria, type I
Reversed 0
HGVS NC_000002.11:g.241818138G>A
CLNSRC
CLNACC RCV000186354.1,