rs78365431
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in complete genomics |
| Make rs78365431(G;T) |
| Make rs78365431(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 12 |
| Position | 40298479 |
| Gene | LRRK2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs78365431 |
| dbSNP (classic) | rs78365431 |
| ClinGen | rs78365431 |
| ebi | rs78365431 |
| HLI | rs78365431 |
| Exac | rs78365431 |
| Gnomad | rs78365431 |
| Varsome | rs78365431 |
| LitVar | rs78365431 |
| Map | rs78365431 |
| PheGenI | rs78365431 |
| Biobank | rs78365431 |
| 1000 genomes | rs78365431 |
| hgdp | rs78365431 |
| ensembl | rs78365431 |
| geneview | rs78365431 |
| scholar | rs78365431 |
| rs78365431 | |
| pharmgkb | rs78365431 |
| gwascentral | rs78365431 |
| openSNP | rs78365431 |
| 23andMe | rs78365431 |
| SNPshot | rs78365431 |
| SNPdbe | rs78365431 |
| MSV3d | rs78365431 |
| GWAS Ctlg | rs78365431 |
| GMAF | 0.002755 |
| Max Magnitude | 0 |
[PMID 21632271
] Lrrk2 p.Q1111H substitution and Parkinson's disease in Latin America
| ClinVar | |
|---|---|
| Risk | rs78365431(T;T) |
| Alt | rs78365431(T;T) |
| Reference | Rs78365431(G;G) |
| Significance | Other |
| Disease | Parkinson disease 8 |
| Variation | info |
| Gene | LRRK2 |
| CLNDBN | Parkinson disease 8, autosomal dominant |
| Reversed | 0 |
| HGVS | NC_000012.11:g.40692281G>T |
| CLNSRC | ClinVar GeneReviews |
| CLNACC | RCV000032437.2, |
