rs509208
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs509208(C;C) |
Make rs509208(C;G) |
Make rs509208(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 3 |
Position | 166296681 |
is a | snp |
is | mentioned by |
dbSNP | rs509208 |
dbSNP (classic) | rs509208 |
ClinGen | rs509208 |
ebi | rs509208 |
HLI | rs509208 |
Exac | rs509208 |
Gnomad | rs509208 |
Varsome | rs509208 |
LitVar | rs509208 |
Map | rs509208 |
PheGenI | rs509208 |
Biobank | rs509208 |
1000 genomes | rs509208 |
hgdp | rs509208 |
ensembl | rs509208 |
geneview | rs509208 |
scholar | rs509208 |
rs509208 | |
pharmgkb | rs509208 |
gwascentral | rs509208 |
openSNP | rs509208 |
23andMe | rs509208 |
SNPshot | rs509208 |
SNPdbe | rs509208 |
MSV3d | rs509208 |
GWAS Ctlg | rs509208 |
GMAF | 0.1703 |
Max Magnitude | 0 |
? | (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 17903298] Genome-wide association with diabetes-related traits in the Framingham Heart Study.