rs987539
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs987539(C;C) |
Make rs987539(C;T) |
Make rs987539(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 7 |
Position | 95407680 |
Gene | PON2 |
is a | snp |
is | mentioned by |
dbSNP | rs987539 |
dbSNP (classic) | rs987539 |
ClinGen | rs987539 |
ebi | rs987539 |
HLI | rs987539 |
Exac | rs987539 |
Gnomad | rs987539 |
Varsome | rs987539 |
LitVar | rs987539 |
Map | rs987539 |
PheGenI | rs987539 |
Biobank | rs987539 |
1000 genomes | rs987539 |
hgdp | rs987539 |
ensembl | rs987539 |
geneview | rs987539 |
scholar | rs987539 |
rs987539 | |
pharmgkb | rs987539 |
gwascentral | rs987539 |
openSNP | rs987539 |
23andMe | rs987539 |
SNPshot | rs987539 |
SNPdbe | rs987539 |
MSV3d | rs987539 |
GWAS Ctlg | rs987539 |
GMAF | 0.3485 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
[PMID 21223581] Association analysis of PON2 genetic variants with serum paraoxonase activity and systemic lupus erythematosus
[PMID 18618303] A common haplotype within the PON1 promoter region is associated with sporadic ALS.