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

rs180177181

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs180177181(C;C)
Make rs180177181(C;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position240869191
GeneAGXT
is asnp
is mentioned by
dbSNPrs180177181
ebirs180177181
HLIrs180177181
Exacrs180177181
Varsomers180177181
Maprs180177181
PheGenIrs180177181
hapmaprs180177181
1000 genomesrs180177181
hgdprs180177181
ensemblrs180177181
gopubmedrs180177181
geneviewrs180177181
scholarrs180177181
googlers180177181
pharmgkbrs180177181
gwascentralrs180177181
openSNPrs180177181
23andMers180177181
23andMe allrs180177181
SNP Nexus

SNPshotrs180177181
SNPdbers180177181
MSV3drs180177181
GWAS Ctlgrs180177181
Max Magnitude0
ClinVar
Risk rs180177181(C;C)
Alt rs180177181(C;C)
Reference rs180177181(G;G)
Significance Pathogenic
Disease Primary hyperoxaluria
Variation info
Gene AGXT
CLNDBN Primary hyperoxaluria, type I
Reversed 0
HGVS NC_000002.11:g.241808608G>C
CLNSRC
CLNACC RCV000186285.1,