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rs180177245

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs180177245(A;G)
Make rs180177245(G;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position240873976
GeneAGXT
is asnp
is mentioned by
dbSNPrs180177245
ebirs180177245
HLIrs180177245
Exacrs180177245
Varsomers180177245
Maprs180177245
PheGenIrs180177245
hapmaprs180177245
1000 genomesrs180177245
hgdprs180177245
ensemblrs180177245
gopubmedrs180177245
geneviewrs180177245
scholarrs180177245
googlers180177245
pharmgkbrs180177245
gwascentralrs180177245
openSNPrs180177245
23andMers180177245
23andMe allrs180177245
SNP Nexus

SNPshotrs180177245
SNPdbers180177245
MSV3drs180177245
GWAS Ctlgrs180177245
Max Magnitude0
ClinVar
Risk rs180177245(G;G)
Alt rs180177245(G;G)
Reference rs180177245(A;A)
Significance Pathogenic
Disease Primary hyperoxaluria
Variation info
Gene AGXT
CLNDBN Primary hyperoxaluria, type I
Reversed 0
HGVS NC_000002.11:g.241813393A>G
CLNSRC
CLNACC RCV000186373.1,