rs6834555
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs6834555(A;A) |
Make rs6834555(A;G) |
Make rs6834555(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 4 |
Position | 10060702 |
is a | snp |
is | mentioned by |
dbSNP | rs6834555 |
dbSNP (classic) | rs6834555 |
ClinGen | rs6834555 |
ebi | rs6834555 |
HLI | rs6834555 |
Exac | rs6834555 |
Gnomad | rs6834555 |
Varsome | rs6834555 |
LitVar | rs6834555 |
Map | rs6834555 |
PheGenI | rs6834555 |
Biobank | rs6834555 |
1000 genomes | rs6834555 |
hgdp | rs6834555 |
ensembl | rs6834555 |
geneview | rs6834555 |
scholar | rs6834555 |
rs6834555 | |
pharmgkb | rs6834555 |
gwascentral | rs6834555 |
openSNP | rs6834555 |
23andMe | rs6834555 |
SNPshot | rs6834555 |
SNPdbe | rs6834555 |
MSV3d | rs6834555 |
GWAS Ctlg | rs6834555 |
GMAF | 0.314 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 22005930![]() |
Trait | |
Title | Genome-wide association study of Alzheimer's disease with psychotic symptoms. |
Risk Allele | |
P-val | 3E-7 |
Odds Ratio | 1.4000 None |