rs6922632
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs6922632(A;A) |
Make rs6922632(A;C) |
Make rs6922632(C;C) |
Reference | GRCh38 38.1/141 |
Chromosome | 6 |
Position | 24106865 |
is a | snp |
is | mentioned by |
dbSNP | rs6922632 |
dbSNP (classic) | rs6922632 |
ClinGen | rs6922632 |
ebi | rs6922632 |
HLI | rs6922632 |
Exac | rs6922632 |
Gnomad | rs6922632 |
Varsome | rs6922632 |
LitVar | rs6922632 |
Map | rs6922632 |
PheGenI | rs6922632 |
Biobank | rs6922632 |
1000 genomes | rs6922632 |
hgdp | rs6922632 |
ensembl | rs6922632 |
geneview | rs6922632 |
scholar | rs6922632 |
rs6922632 | |
pharmgkb | rs6922632 |
gwascentral | rs6922632 |
openSNP | rs6922632 |
23andMe | rs6922632 |
SNPshot | rs6922632 |
SNPdbe | rs6922632 |
MSV3d | rs6922632 |
GWAS Ctlg | rs6922632 |
GMAF | 0.118 |
Max Magnitude | 0 |
? | (A;A) (A;C) (C;C) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 21130836![]() |
Trait | |
Title | Whole genome association scan for genetic polymorphisms influencing information processing speed |
Risk Allele | A |
P-val | 0.000004 |
Odds Ratio | 0.1900 [0.11-0.27] unit increase |