rs1136666
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs1136666(C;C) |
| Make rs1136666(C;G) |
| Make rs1136666(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 12 |
| Position | 6534825 |
| Gene | GAPDH |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1136666 |
| dbSNP (classic) | rs1136666 |
| ClinGen | rs1136666 |
| ebi | rs1136666 |
| HLI | rs1136666 |
| Exac | rs1136666 |
| Gnomad | rs1136666 |
| Varsome | rs1136666 |
| LitVar | rs1136666 |
| Map | rs1136666 |
| PheGenI | rs1136666 |
| Biobank | rs1136666 |
| 1000 genomes | rs1136666 |
| hgdp | rs1136666 |
| ensembl | rs1136666 |
| geneview | rs1136666 |
| scholar | rs1136666 |
| rs1136666 | |
| pharmgkb | rs1136666 |
| gwascentral | rs1136666 |
| openSNP | rs1136666 |
| 23andMe | rs1136666 |
| SNPshot | rs1136666 |
| SNPdbe | rs1136666 |
| MSV3d | rs1136666 |
| GWAS Ctlg | rs1136666 |
| Merged from | Rs3741916 |
| GMAF | 0.2548 |
| Max Magnitude | 0 |
| ? | (C;C) (C;G) (G;G) | 28 |
|---|---|---|
|
| ||
[PMID 15507493
] Association of late-onset Alzheimer's disease with genetic variation in multiple members of the GAPD gene family.
[PMID 18340469] Further examination of the candidate genes in chromosome 12p13 locus for late-onset Alzheimer disease.
[PMID 20864222] Association and heterogeneity at the GAPDH locus in Alzheimer's disease.
[PMID 29886133] GAPDH rs1136666 SNP indicates a high risk of Parkinson's disease.
