rs616338
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Reference | GRCh38.p7 38.3/150 |
| Chromosome | 17 |
| Position | 49219935 |
| Gene | ABI3 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs616338 |
| dbSNP (classic) | rs616338 |
| ClinGen | rs616338 |
| ebi | rs616338 |
| HLI | rs616338 |
| Exac | rs616338 |
| Gnomad | rs616338 |
| Varsome | rs616338 |
| LitVar | rs616338 |
| Map | rs616338 |
| PheGenI | rs616338 |
| Biobank | rs616338 |
| 1000 genomes | rs616338 |
| hgdp | rs616338 |
| ensembl | rs616338 |
| geneview | rs616338 |
| scholar | rs616338 |
| rs616338 | |
| pharmgkb | rs616338 |
| gwascentral | rs616338 |
| openSNP | rs616338 |
| 23andMe | rs616338 |
| SNPshot | rs616338 |
| SNPdbe | rs616338 |
| MSV3d | rs616338 |
| GWAS Ctlg | rs616338 |
| Max Magnitude | 0 |
rs616338 (p.Ser209Phe) is risk variant in the ABI3 gene reported to be associated with a moderate increase in risk for Alzheimer's disease. (P = 4.56 × 10-10, OR = 1.43). It is involved in immune interaction through microglia.[PMID 28714976
]
