rs7133914
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in complete genomics |
| Make rs7133914(A;A) |
| Make rs7133914(A;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 12 |
| Position | 40309109 |
| Gene | LRRK2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs7133914 |
| dbSNP (classic) | rs7133914 |
| ClinGen | rs7133914 |
| ebi | rs7133914 |
| HLI | rs7133914 |
| Exac | rs7133914 |
| Gnomad | rs7133914 |
| Varsome | rs7133914 |
| LitVar | rs7133914 |
| Map | rs7133914 |
| PheGenI | rs7133914 |
| Biobank | rs7133914 |
| 1000 genomes | rs7133914 |
| hgdp | rs7133914 |
| ensembl | rs7133914 |
| geneview | rs7133914 |
| scholar | rs7133914 |
| rs7133914 | |
| pharmgkb | rs7133914 |
| gwascentral | rs7133914 |
| openSNP | rs7133914 |
| 23andMe | rs7133914 |
| SNPshot | rs7133914 |
| SNPdbe | rs7133914 |
| MSV3d | rs7133914 |
| GWAS Ctlg | rs7133914 |
| GMAF | 0.09963 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
[PMID 18952485
] Haplotype analysis of Lrrk2 R1441H carriers with parkinsonism.
[PMID 20186690] Multiple LRRK2 variants modulate risk of Parkinson disease: a Chinese multicenter study.
[PMID 23962496] The protective effect of LRRK2 p.R1398H on risk of Parkinson's disease is independent of MAPT and SNCA variants
| ClinVar | |
|---|---|
| Risk | rs7133914(A;A) rs7133914(T;T) |
| Alt | rs7133914(A;A) rs7133914(T;T) |
| Reference | Rs7133914(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.40702911G>A |
| CLNSRC | UniProtKB (protein) |
| CLNACC | RCV000032452.2, |
