rs7687945
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs7687945(C;C) |
| Make rs7687945(C;T) |
| Make rs7687945(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 4 |
| Position | 89843548 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs7687945 |
| dbSNP (classic) | rs7687945 |
| ClinGen | rs7687945 |
| ebi | rs7687945 |
| HLI | rs7687945 |
| Exac | rs7687945 |
| Gnomad | rs7687945 |
| Varsome | rs7687945 |
| LitVar | rs7687945 |
| Map | rs7687945 |
| PheGenI | rs7687945 |
| Biobank | rs7687945 |
| 1000 genomes | rs7687945 |
| hgdp | rs7687945 |
| ensembl | rs7687945 |
| geneview | rs7687945 |
| scholar | rs7687945 |
| rs7687945 | |
| pharmgkb | rs7687945 |
| gwascentral | rs7687945 |
| openSNP | rs7687945 |
| 23andMe | rs7687945 |
| SNPshot | rs7687945 |
| SNPdbe | rs7687945 |
| MSV3d | rs7687945 |
| GWAS Ctlg | rs7687945 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
"Dissection of the genetics of Parkinson's disease identifies an additional association 5′ of SNCA and multiple associated haplotypes at 17q21" [PMID 21044948
] suggests this is Parkinson's Disease associated together with rs356220, masked in other GWAS by rs2736990 via Simpson's paradox. Association replicated in French dataset with r^2 0.98 LD rs2301134 substituted.
