rs284495
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs284495(C;C) |
Make rs284495(C;T) |
Make rs284495(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 8 |
Position | 104953350 |
is a | snp |
is | mentioned by |
dbSNP | rs284495 |
dbSNP (classic) | rs284495 |
ClinGen | rs284495 |
ebi | rs284495 |
HLI | rs284495 |
Exac | rs284495 |
Gnomad | rs284495 |
Varsome | rs284495 |
LitVar | rs284495 |
Map | rs284495 |
PheGenI | rs284495 |
Biobank | rs284495 |
1000 genomes | rs284495 |
hgdp | rs284495 |
ensembl | rs284495 |
geneview | rs284495 |
scholar | rs284495 |
rs284495 | |
pharmgkb | rs284495 |
gwascentral | rs284495 |
openSNP | rs284495 |
23andMe | rs284495 |
SNPshot | rs284495 |
SNPdbe | rs284495 |
MSV3d | rs284495 |
GWAS Ctlg | rs284495 |
GMAF | 0.4467 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
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[PMID 22570617] Common Variants at 9p21 and 8q22 Are Associated with Increased Susceptibility to Optic Nerve Degeneration in Glaucoma
[PMID 17903300] Genome-wide association to body mass index and waist circumference: the Framingham Heart Study 100K project.