Have questions? Visit https://www.reddit.com/r/SNPedia

rs180177268

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs180177268(C;C)
Make rs180177268(C;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position240868942
GeneAGXT
is asnp
is mentioned by
dbSNPrs180177268
ebirs180177268
HLIrs180177268
Exacrs180177268
Varsomers180177268
Maprs180177268
PheGenIrs180177268
hapmaprs180177268
1000 genomesrs180177268
hgdprs180177268
ensemblrs180177268
gopubmedrs180177268
geneviewrs180177268
scholarrs180177268
googlers180177268
pharmgkbrs180177268
gwascentralrs180177268
openSNPrs180177268
23andMers180177268
23andMe allrs180177268
SNP Nexus

SNPshotrs180177268
SNPdbers180177268
MSV3drs180177268
GWAS Ctlgrs180177268
Max Magnitude0
ClinVar
Risk rs180177268(C;C)
Alt rs180177268(C;C)
Reference rs180177268(T;T)
Significance Pathogenic
Disease Primary hyperoxaluria
Variation info
Gene AGXT
CLNDBN Primary hyperoxaluria, type I
Reversed 0
HGVS NC_000002.11:g.241808359T>C
CLNSRC
CLNACC RCV000186277.1,