rs66737902
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (T;T) | 0 | common in clinvar |
| Make rs66737902(C;C) |
| Make rs66737902(C;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 12 |
| Position | 40367861 |
| Gene | LOC105369736, LRRK2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs66737902 |
| dbSNP (classic) | rs66737902 |
| ClinGen | rs66737902 |
| ebi | rs66737902 |
| HLI | rs66737902 |
| Exac | rs66737902 |
| Gnomad | rs66737902 |
| Varsome | rs66737902 |
| LitVar | rs66737902 |
| Map | rs66737902 |
| PheGenI | rs66737902 |
| Biobank | rs66737902 |
| 1000 genomes | rs66737902 |
| hgdp | rs66737902 |
| ensembl | rs66737902 |
| geneview | rs66737902 |
| scholar | rs66737902 |
| rs66737902 | |
| pharmgkb | rs66737902 |
| gwascentral | rs66737902 |
| openSNP | rs66737902 |
| 23andMe | rs66737902 |
| SNPshot | rs66737902 |
| SNPdbe | rs66737902 |
| MSV3d | rs66737902 |
| GWAS Ctlg | rs66737902 |
| Max Magnitude | 0 |
[PMID 24758914] The screening of the 3'UTR sequence of LRRK2 identified an association between the rs66737902 polymorphism and Parkinson's disease
| ClinVar | |
|---|---|
| Risk | rs66737902(C;C) |
| Alt | rs66737902(C;C) |
| Reference | Rs66737902(T;T) |
| Significance | Probable-non-pathogenic |
| Disease | Parkinson disease 8 |
| Variation | info |
| Gene | LRRK2 |
| CLNDBN | Parkinson disease 8, autosomal dominant |
| Reversed | 0 |
| HGVS | NC_000012.11:g.40761663T>C |
| CLNSRC | |
| CLNACC | RCV000371980.1, |
