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

rs180177234

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs180177234(A;A)
Make rs180177234(A;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position240872978
GeneAGXT
is asnp
is mentioned by
dbSNPrs180177234
ebirs180177234
HLIrs180177234
Exacrs180177234
Varsomers180177234
Maprs180177234
PheGenIrs180177234
hapmaprs180177234
1000 genomesrs180177234
hgdprs180177234
ensemblrs180177234
gopubmedrs180177234
geneviewrs180177234
scholarrs180177234
googlers180177234
pharmgkbrs180177234
gwascentralrs180177234
openSNPrs180177234
23andMers180177234
23andMe allrs180177234
SNP Nexus

SNPshotrs180177234
SNPdbers180177234
MSV3drs180177234
GWAS Ctlgrs180177234
Max Magnitude0
ClinVar
Risk rs180177234(A;A)
Alt rs180177234(A;A)
Reference rs180177234(G;G)
Significance Pathogenic
Disease Primary hyperoxaluria
Variation info
Gene AGXT
CLNDBN Primary hyperoxaluria, type I
Reversed 0
HGVS NC_000002.11:g.241812395G>A
CLNSRC
CLNACC RCV000186372.1,