rs3764640
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs3764640(G;T) |
Make rs3764640(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 19 |
Position | 1207239 |
Gene | STK11 |
is a | snp |
is | mentioned by |
dbSNP | rs3764640 |
dbSNP (classic) | rs3764640 |
ClinGen | rs3764640 |
ebi | rs3764640 |
HLI | rs3764640 |
Exac | rs3764640 |
Gnomad | rs3764640 |
Varsome | rs3764640 |
LitVar | rs3764640 |
Map | rs3764640 |
PheGenI | rs3764640 |
Biobank | rs3764640 |
1000 genomes | rs3764640 |
hgdp | rs3764640 |
ensembl | rs3764640 |
geneview | rs3764640 |
scholar | rs3764640 |
rs3764640 | |
pharmgkb | rs3764640 |
gwascentral | rs3764640 |
openSNP | rs3764640 |
23andMe | rs3764640 |
SNPshot | rs3764640 |
SNPdbe | rs3764640 |
MSV3d | rs3764640 |
GWAS Ctlg | rs3764640 |
GMAF | 0.359 |
Max Magnitude | 0 |
? | (G;G) (G;T) (T;T) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 22005930![]() |
Trait | |
Title | Genome-wide association study of Alzheimer's disease with psychotic symptoms. |
Risk Allele | |
P-val | 0.000008 |
Odds Ratio | 1.4700 None |
ClinVar | |
---|---|
Risk | rs3764640(T;T) |
Alt | rs3764640(T;T) |
Reference | Rs3764640(G;G) |
Significance | Non-pathogenic |
Disease | not specified |
Variation | info |
Gene | STK11 |
CLNDBN | not specified |
Reversed | 0 |
HGVS | NC_000019.9:g.1207238G>T |
CLNSRC | |
CLNACC | RCV000254173.1, |