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

rs180177266

From SNPedia

Merged intors180177265
Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs180177266(C;C)
Make rs180177266(C;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position240875205
GeneAGXT
is asnp
is mentioned by
dbSNPrs180177266
ebirs180177266
HLIrs180177266
Exacrs180177266
Varsomers180177266
Maprs180177266
PheGenIrs180177266
hapmaprs180177266
1000 genomesrs180177266
hgdprs180177266
ensemblrs180177266
gopubmedrs180177266
geneviewrs180177266
scholarrs180177266
googlers180177266
pharmgkbrs180177266
gwascentralrs180177266
openSNPrs180177266
23andMers180177266
23andMe allrs180177266
SNP Nexus

SNPshotrs180177266
SNPdbers180177266
MSV3drs180177266
GWAS Ctlgrs180177266
StatusMerged into rs180177265
Max Magnitude0
ClinVar
Risk rs180177266(C;C)
Alt rs180177266(C;C)
Reference rs180177266(G;G)
Significance Pathogenic
Disease
Variation info
Gene AGXT
CLNDBN OMIM
Reversed 0
HGVS NC_000002.11:g.241814622G>C
CLNSRC
CLNACC