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

rs180177249

From SNPedia

Merged intors180177248
Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs180177249(C;T)
Make rs180177249(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position240873996
GeneAGXT
is asnp
is mentioned by
dbSNPrs180177249
ebirs180177249
HLIrs180177249
Exacrs180177249
Varsomers180177249
Maprs180177249
PheGenIrs180177249
hapmaprs180177249
1000 genomesrs180177249
hgdprs180177249
ensemblrs180177249
gopubmedrs180177249
geneviewrs180177249
scholarrs180177249
googlers180177249
pharmgkbrs180177249
gwascentralrs180177249
openSNPrs180177249
23andMers180177249
23andMe allrs180177249
SNP Nexus

SNPshotrs180177249
SNPdbers180177249
MSV3drs180177249
GWAS Ctlgrs180177249
StatusMerged into rs180177248
Max Magnitude0
ClinVar
Risk rs180177249(T;T)
Alt rs180177249(T;T)
Reference rs180177249(C;C)
Significance Pathogenic
Disease
Variation info
Gene AGXT
CLNDBN OMIM
Reversed 0
HGVS NC_000002.11:g.241813413C>T
CLNSRC
CLNACC