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

rs180177251

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(TCCA;TCCA) 0 common in clinvar
Make rs180177251(-;-)
Make rs180177251(-;TCCA)
ReferenceGRCh38 38.1/141
Chromosome2
Position240874024
GeneAGXT
is asnp
is mentioned by
dbSNPrs180177251
ebirs180177251
HLIrs180177251
Exacrs180177251
Varsomers180177251
Maprs180177251
PheGenIrs180177251
hapmaprs180177251
1000 genomesrs180177251
hgdprs180177251
ensemblrs180177251
gopubmedrs180177251
geneviewrs180177251
scholarrs180177251
googlers180177251
pharmgkbrs180177251
gwascentralrs180177251
openSNPrs180177251
23andMers180177251
23andMe allrs180177251
SNP Nexus

SNPshotrs180177251
SNPdbers180177251
MSV3drs180177251
GWAS Ctlgrs180177251
Max Magnitude0
ClinVar
Risk rs180177251(;)
Alt rs180177251(;)
Reference rs180177251(TCCA;TCCA)
Significance Pathogenic
Disease Primary hyperoxaluria
Variation info
Gene AGXT
CLNDBN Primary hyperoxaluria, type I
Reversed 0
HGVS NC_000002.11:g.241813441_241813444delTCCA
CLNSRC
CLNACC RCV000186400.1,