rs17884563
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs17884563(A;A) |
Make rs17884563(A;T) |
Make rs17884563(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 7 |
Position | 95400715 |
is a | snp |
is | mentioned by |
dbSNP | rs17884563 |
dbSNP (classic) | rs17884563 |
ClinGen | rs17884563 |
ebi | rs17884563 |
HLI | rs17884563 |
Exac | rs17884563 |
Gnomad | rs17884563 |
Varsome | rs17884563 |
LitVar | rs17884563 |
Map | rs17884563 |
PheGenI | rs17884563 |
Biobank | rs17884563 |
1000 genomes | rs17884563 |
hgdp | rs17884563 |
ensembl | rs17884563 |
geneview | rs17884563 |
scholar | rs17884563 |
rs17884563 | |
pharmgkb | rs17884563 |
gwascentral | rs17884563 |
openSNP | rs17884563 |
23andMe | rs17884563 |
SNPshot | rs17884563 |
SNPdbe | rs17884563 |
MSV3d | rs17884563 |
GWAS Ctlg | rs17884563 |
GMAF | 0.09045 |
Max Magnitude | 0 |
[PMID 21223581] Association analysis of PON2 genetic variants with serum paraoxonase activity and systemic lupus erythematosus