rs10495669
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs10495669(C;C) |
Make rs10495669(C;G) |
Make rs10495669(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 2 |
Position | 17844006 |
Gene | ZPAXP |
is a | snp |
is | mentioned by |
dbSNP | rs10495669 |
dbSNP (classic) | rs10495669 |
ClinGen | rs10495669 |
ebi | rs10495669 |
HLI | rs10495669 |
Exac | rs10495669 |
Gnomad | rs10495669 |
Varsome | rs10495669 |
LitVar | rs10495669 |
Map | rs10495669 |
PheGenI | rs10495669 |
Biobank | rs10495669 |
1000 genomes | rs10495669 |
hgdp | rs10495669 |
ensembl | rs10495669 |
geneview | rs10495669 |
scholar | rs10495669 |
rs10495669 | |
pharmgkb | rs10495669 |
gwascentral | rs10495669 |
openSNP | rs10495669 |
23andMe | rs10495669 |
SNPshot | rs10495669 |
SNPdbe | rs10495669 |
MSV3d | rs10495669 |
GWAS Ctlg | rs10495669 |
GMAF | 0.3958 |
Max Magnitude | 0 |
? | (C;C) (C;G) (G;G) | 28 |
---|---|---|
|
[PMID 17903299] A genome-wide association study for blood lipid phenotypes in the Framingham Heart Study.