rs9985399
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in complete genomics |
Make rs9985399(C;C) |
Make rs9985399(C;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 3 |
Position | 39967143 |
Gene | MYRIP |
is a | snp |
is | mentioned by |
dbSNP | rs9985399 |
dbSNP (classic) | rs9985399 |
ClinGen | rs9985399 |
ebi | rs9985399 |
HLI | rs9985399 |
Exac | rs9985399 |
Gnomad | rs9985399 |
Varsome | rs9985399 |
LitVar | rs9985399 |
Map | rs9985399 |
PheGenI | rs9985399 |
Biobank | rs9985399 |
1000 genomes | rs9985399 |
hgdp | rs9985399 |
ensembl | rs9985399 |
geneview | rs9985399 |
scholar | rs9985399 |
rs9985399 | |
pharmgkb | rs9985399 |
gwascentral | rs9985399 |
openSNP | rs9985399 |
23andMe | rs9985399 |
SNPshot | rs9985399 |
SNPdbe | rs9985399 |
MSV3d | rs9985399 |
GWAS Ctlg | rs9985399 |
GMAF | 0.2259 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 21130836] |
Trait | |
Title | Whole genome association scan for genetic polymorphisms influencing information processing speed |
Risk Allele | T |
P-val | 0.000009 |
Odds Ratio | 0.2600 [0.14-0.38] unit decrease |