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rs180177250

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs180177250(C;C)
Make rs180177250(C;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position240874010
GeneAGXT
is asnp
is mentioned by
dbSNPrs180177250
ebirs180177250
HLIrs180177250
Exacrs180177250
Varsomers180177250
Maprs180177250
PheGenIrs180177250
hapmaprs180177250
1000 genomesrs180177250
hgdprs180177250
ensemblrs180177250
gopubmedrs180177250
geneviewrs180177250
scholarrs180177250
googlers180177250
pharmgkbrs180177250
gwascentralrs180177250
openSNPrs180177250
23andMers180177250
23andMe allrs180177250
SNP Nexus

SNPshotrs180177250
SNPdbers180177250
MSV3drs180177250
GWAS Ctlgrs180177250
Max Magnitude0
ClinVar
Risk rs180177250(C;C)
Alt rs180177250(C;C)
Reference rs180177250(G;G)
Significance Pathogenic
Disease Primary hyperoxaluria
Variation info
Gene AGXT
CLNDBN Primary hyperoxaluria, type I
Reversed 0
HGVS NC_000002.11:g.241813427G>C
CLNSRC
CLNACC RCV000186326.1,