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rs180177162

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs180177162(A;A)
Make rs180177162(A;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position240868972
GeneAGXT
is asnp
is mentioned by
dbSNPrs180177162
ebirs180177162
HLIrs180177162
Exacrs180177162
Varsomers180177162
Maprs180177162
PheGenIrs180177162
hapmaprs180177162
1000 genomesrs180177162
hgdprs180177162
ensemblrs180177162
gopubmedrs180177162
geneviewrs180177162
scholarrs180177162
googlers180177162
pharmgkbrs180177162
gwascentralrs180177162
openSNPrs180177162
23andMers180177162
23andMe allrs180177162
SNP Nexus

SNPshotrs180177162
SNPdbers180177162
MSV3drs180177162
GWAS Ctlgrs180177162
Max Magnitude0
ClinVar
Risk rs180177162(A;A)
Alt rs180177162(A;A)
Reference rs180177162(G;G)
Significance Pathogenic
Disease Primary hyperoxaluria
Variation info
Gene AGXT
CLNDBN Primary hyperoxaluria, type I
Reversed 0
HGVS NC_000002.11:g.241808389G>A
CLNSRC
CLNACC RCV000186278.1,