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rs180177286

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs180177286(C;G)
Make rs180177286(G;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position240877534
GeneAGXT
is asnp
is mentioned by
dbSNPrs180177286
ebirs180177286
HLIrs180177286
Exacrs180177286
Varsomers180177286
Maprs180177286
PheGenIrs180177286
hapmaprs180177286
1000 genomesrs180177286
hgdprs180177286
ensemblrs180177286
gopubmedrs180177286
geneviewrs180177286
scholarrs180177286
googlers180177286
pharmgkbrs180177286
gwascentralrs180177286
openSNPrs180177286
23andMers180177286
23andMe allrs180177286
SNP Nexus

SNPshotrs180177286
SNPdbers180177286
MSV3drs180177286
GWAS Ctlgrs180177286
Max Magnitude0
ClinVar
Risk rs180177286(G,T;G,T)
Alt rs180177286(G,T;G,T)
Reference rs180177286(C;C)
Significance Pathogenic
Disease Primary hyperoxaluria
Variation info
Gene AGXT
CLNDBN Primary hyperoxaluria, type I
Reversed 0
HGVS NC_000002.11:g.241816951C>G
CLNSRC
CLNACC RCV000186376.1,