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rs180177241

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs180177241(-;-)
Make rs180177241(-;C)
ReferenceGRCh38 38.1/141
Chromosome2
Position240873031
GeneAGXT
is asnp
is mentioned by
dbSNPrs180177241
ebirs180177241
HLIrs180177241
Exacrs180177241
Varsomers180177241
Maprs180177241
PheGenIrs180177241
hapmaprs180177241
1000 genomesrs180177241
hgdprs180177241
ensemblrs180177241
gopubmedrs180177241
geneviewrs180177241
scholarrs180177241
googlers180177241
pharmgkbrs180177241
gwascentralrs180177241
openSNPrs180177241
23andMers180177241
23andMe allrs180177241
SNP Nexus

SNPshotrs180177241
SNPdbers180177241
MSV3drs180177241
GWAS Ctlgrs180177241
Max Magnitude0
ClinVar
Risk rs180177241(;)
Alt rs180177241(;)
Reference rs180177241(C;C)
Significance Pathogenic
Disease Primary hyperoxaluria
Variation info
Gene AGXT
CLNDBN Primary hyperoxaluria, type I
Reversed 0
HGVS NC_000002.11:g.241812448delC
CLNSRC
CLNACC RCV000186398.1,