rs704180
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs704180(A;A) |
| Make rs704180(A;G) |
| Make rs704180(G;G) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 12 |
| Position | 21841177 |
| Gene | ABCC9 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs704180 |
| dbSNP (classic) | rs704180 |
| ClinGen | rs704180 |
| ebi | rs704180 |
| HLI | rs704180 |
| Exac | rs704180 |
| Gnomad | rs704180 |
| Varsome | rs704180 |
| LitVar | rs704180 |
| Map | rs704180 |
| PheGenI | rs704180 |
| Biobank | rs704180 |
| 1000 genomes | rs704180 |
| hgdp | rs704180 |
| ensembl | rs704180 |
| geneview | rs704180 |
| scholar | rs704180 |
| rs704180 | |
| pharmgkb | rs704180 |
| gwascentral | rs704180 |
| openSNP | rs704180 |
| 23andMe | rs704180 |
| SNPshot | rs704180 |
| SNPdbe | rs704180 |
| MSV3d | rs704180 |
| GWAS Ctlg | rs704180 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
[PMID 25470345
] Reassessment of risk genotypes (GRN, TMEM106B, and ABCC9 variants) associated with hippocampal sclerosis of aging pathology
[PMID 26115089] Novel human ABCC9/SUR2 brain expressed transcripts and an eQTL relevant to hippocampal sclerosis of aging
[PMID 28189700] CSF protein changes associated with hippocampal sclerosis risk gene variants highlight impact of GRN/PGRN.
