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rs180177294

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs180177294(C;T)
Make rs180177294(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position240877597
GeneAGXT
is asnp
is mentioned by
dbSNPrs180177294
ebirs180177294
HLIrs180177294
Exacrs180177294
Varsomers180177294
Maprs180177294
PheGenIrs180177294
hapmaprs180177294
1000 genomesrs180177294
hgdprs180177294
ensemblrs180177294
gopubmedrs180177294
geneviewrs180177294
scholarrs180177294
googlers180177294
pharmgkbrs180177294
gwascentralrs180177294
openSNPrs180177294
23andMers180177294
23andMe allrs180177294
SNP Nexus

SNPshotrs180177294
SNPdbers180177294
MSV3drs180177294
GWAS Ctlgrs180177294
Max Magnitude0
ClinVar
Risk rs180177294(T;T)
Alt rs180177294(T;T)
Reference rs180177294(C;C)
Significance Pathogenic
Disease Primary hyperoxaluria
Variation info
Gene AGXT
CLNDBN Primary hyperoxaluria, type I
Reversed 0
HGVS NC_000002.11:g.241817014C>T
CLNSRC
CLNACC RCV000186344.1,