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rs180177298

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs180177298(G;T)
Make rs180177298(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position240878021
GeneAGXT
is asnp
is mentioned by
dbSNPrs180177298
ebirs180177298
HLIrs180177298
Exacrs180177298
Varsomers180177298
Maprs180177298
PheGenIrs180177298
hapmaprs180177298
1000 genomesrs180177298
hgdprs180177298
ensemblrs180177298
gopubmedrs180177298
geneviewrs180177298
scholarrs180177298
googlers180177298
pharmgkbrs180177298
gwascentralrs180177298
openSNPrs180177298
23andMers180177298
23andMe allrs180177298
SNP Nexus

SNPshotrs180177298
SNPdbers180177298
MSV3drs180177298
GWAS Ctlgrs180177298
Max Magnitude0
ClinVar
Risk rs180177298(T;T)
Alt rs180177298(T;T)
Reference rs180177298(G;G)
Significance Pathogenic
Disease Primary hyperoxaluria
Variation info
Gene AGXT
CLNDBN Primary hyperoxaluria, type I
Reversed 0
HGVS NC_000002.11:g.241817438G>A; NC_000002.11:g.241817438G>T
CLNSRC
CLNACC RCV000186378.1, RCV000186377.1,