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rs180177204

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs180177204(A;A)
Make rs180177204(A;C)
ReferenceGRCh38 38.1/141
Chromosome2
Position240869340
GeneAGXT
is asnp
is mentioned by
dbSNPrs180177204
ebirs180177204
HLIrs180177204
Exacrs180177204
Varsomers180177204
Maprs180177204
PheGenIrs180177204
hapmaprs180177204
1000 genomesrs180177204
hgdprs180177204
ensemblrs180177204
gopubmedrs180177204
geneviewrs180177204
scholarrs180177204
googlers180177204
pharmgkbrs180177204
gwascentralrs180177204
openSNPrs180177204
23andMers180177204
23andMe allrs180177204
SNP Nexus

SNPshotrs180177204
SNPdbers180177204
MSV3drs180177204
GWAS Ctlgrs180177204
Max Magnitude0
ClinVar
Risk rs180177204(A;A)
Alt rs180177204(A;A)
Reference rs180177204(C;C)
Significance Pathogenic
Disease Primary hyperoxaluria
Variation info
Gene AGXT
CLNDBN Primary hyperoxaluria, type I
Reversed 0
HGVS NC_000002.11:g.241808757C>A
CLNSRC
CLNACC