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rs180177228

From SNPedia

Merged intors180177227
Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs180177228(C;C)
Make rs180177228(C;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position240871406
GeneAGXT
is asnp
is mentioned by
dbSNPrs180177228
ebirs180177228
HLIrs180177228
Exacrs180177228
Varsomers180177228
Maprs180177228
PheGenIrs180177228
hapmaprs180177228
1000 genomesrs180177228
hgdprs180177228
ensemblrs180177228
gopubmedrs180177228
geneviewrs180177228
scholarrs180177228
googlers180177228
pharmgkbrs180177228
gwascentralrs180177228
openSNPrs180177228
23andMers180177228
23andMe allrs180177228
SNP Nexus

SNPshotrs180177228
SNPdbers180177228
MSV3drs180177228
GWAS Ctlgrs180177228
StatusMerged into rs180177227
Max Magnitude0
ClinVar
Risk rs180177228(C;C)
Alt rs180177228(C;C)
Reference rs180177228(G;G)
Significance Pathogenic
Disease
Variation info
Gene AGXT
CLNDBN OMIM
Reversed 0
HGVS NC_000002.11:g.241810823G>C
CLNSRC
CLNACC