rs8106822
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs8106822(A;A) |
Make rs8106822(A;G) |
Make rs8106822(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 19 |
Position | 31373516 |
Gene | LOC107985311 |
is a | snp |
is | mentioned by |
dbSNP | rs8106822 |
dbSNP (classic) | rs8106822 |
ClinGen | rs8106822 |
ebi | rs8106822 |
HLI | rs8106822 |
Exac | rs8106822 |
Gnomad | rs8106822 |
Varsome | rs8106822 |
LitVar | rs8106822 |
Map | rs8106822 |
PheGenI | rs8106822 |
Biobank | rs8106822 |
1000 genomes | rs8106822 |
hgdp | rs8106822 |
ensembl | rs8106822 |
geneview | rs8106822 |
scholar | rs8106822 |
rs8106822 | |
pharmgkb | rs8106822 |
gwascentral | rs8106822 |
openSNP | rs8106822 |
23andMe | rs8106822 |
SNPshot | rs8106822 |
SNPdbe | rs8106822 |
MSV3d | rs8106822 |
GWAS Ctlg | rs8106822 |
GMAF | 0.4582 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 19808960] Apolipoprotein E/C1 Locus Variants Modify Renal Cell Carcinoma Risk