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rs180177299

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs180177299(C;T)
Make rs180177299(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position240878035
GeneAGXT
is asnp
is mentioned by
dbSNPrs180177299
ebirs180177299
HLIrs180177299
Exacrs180177299
Varsomers180177299
Maprs180177299
PheGenIrs180177299
hapmaprs180177299
1000 genomesrs180177299
hgdprs180177299
ensemblrs180177299
gopubmedrs180177299
geneviewrs180177299
scholarrs180177299
googlers180177299
pharmgkbrs180177299
gwascentralrs180177299
openSNPrs180177299
23andMers180177299
23andMe allrs180177299
SNP Nexus

SNPshotrs180177299
SNPdbers180177299
MSV3drs180177299
GWAS Ctlgrs180177299
Max Magnitude0
ClinVar
Risk rs180177299(T;T)
Alt rs180177299(T;T)
Reference rs180177299(C;C)
Significance Pathogenic
Disease Primary hyperoxaluria
Variation info
Gene AGXT
CLNDBN Primary hyperoxaluria, type I
Reversed 0
HGVS NC_000002.11:g.241817452C>T
CLNSRC
CLNACC RCV000186347.1,