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rs509208

From SNPedia

Orientationplus
Stabilizedplus
Make rs509208(C;C)
Make rs509208(C;G)
Make rs509208(G;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position166296681
is asnp
is mentioned by
dbSNPrs509208
ebirs509208
HLIrs509208
Exacrs509208
Varsomers509208
Maprs509208
PheGenIrs509208
hapmaprs509208
1000 genomesrs509208
hgdprs509208
ensemblrs509208
gopubmedrs509208
geneviewrs509208
scholarrs509208
googlers509208
pharmgkbrs509208
gwascentralrs509208
openSNPrs509208
23andMers509208
23andMe allrs509208
SNP Nexus

SNPshotrs509208
SNPdbers509208
MSV3drs509208
GWAS Ctlgrs509208
GMAF0.1703
Max Magnitude
? (C;C) (C;G) (G;G) 28
This SNP, on chromosome 3 upstream of BCHE (butyrylcholinesterase), is associated with higher cerebral amyloid deposition. The risk allele is G.

[PMID 23419831OA-icon.png]

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[PMID 17903298OA-icon.png] Genome-wide association with diabetes-related traits in the Framingham Heart Study.