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rs180177225

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs180177225(A;A)
Make rs180177225(A;C)
ReferenceGRCh38 38.1/141
Chromosome2
Position240871398
GeneAGXT
is asnp
is mentioned by
dbSNPrs180177225
ebirs180177225
HLIrs180177225
Exacrs180177225
Varsomers180177225
Maprs180177225
PheGenIrs180177225
hapmaprs180177225
1000 genomesrs180177225
hgdprs180177225
ensemblrs180177225
gopubmedrs180177225
geneviewrs180177225
scholarrs180177225
googlers180177225
pharmgkbrs180177225
gwascentralrs180177225
openSNPrs180177225
23andMers180177225
23andMe allrs180177225
SNP Nexus

SNPshotrs180177225
SNPdbers180177225
MSV3drs180177225
GWAS Ctlgrs180177225
Merged fromRs180177226
Max Magnitude0
ClinVar
Risk rs180177225(A,T;A,T)
Alt rs180177225(A,T;A,T)
Reference rs180177225(C;C)
Significance Pathogenic
Disease Primary hyperoxaluria
Variation info
Gene AGXT
CLNDBN Primary hyperoxaluria, type I
Reversed 0
HGVS NC_000002.11:g.241810815C>A; NC_000002.11:g.241810815C>T
CLNSRC
CLNACC RCV000186310.1, RCV000186309.1,