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

rs180177208

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs180177208(G;T)
Make rs180177208(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position240869353
GeneAGXT
is asnp
is mentioned by
dbSNPrs180177208
ebirs180177208
HLIrs180177208
Exacrs180177208
Varsomers180177208
Maprs180177208
PheGenIrs180177208
hapmaprs180177208
1000 genomesrs180177208
hgdprs180177208
ensemblrs180177208
gopubmedrs180177208
geneviewrs180177208
scholarrs180177208
googlers180177208
pharmgkbrs180177208
gwascentralrs180177208
openSNPrs180177208
23andMers180177208
23andMe allrs180177208
SNP Nexus

SNPshotrs180177208
SNPdbers180177208
MSV3drs180177208
GWAS Ctlgrs180177208
Max Magnitude0
ClinVar
Risk rs180177208(T;T)
Alt rs180177208(T;T)
Reference rs180177208(G;G)
Significance Pathogenic
Disease Primary hyperoxaluria
Variation info
Gene AGXT
CLNDBN Primary hyperoxaluria, type I
Reversed 0
HGVS NC_000002.11:g.241808770G>T
CLNSRC
CLNACC RCV000186300.1,