rs1801334
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in clinvar |
| Make rs1801334(A;A) |
| Make rs1801334(A;G) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 6 |
| Position | 161360193 |
| Gene | PARK2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1801334 |
| dbSNP (classic) | rs1801334 |
| ClinGen | rs1801334 |
| ebi | rs1801334 |
| HLI | rs1801334 |
| Exac | rs1801334 |
| Gnomad | rs1801334 |
| Varsome | rs1801334 |
| LitVar | rs1801334 |
| Map | rs1801334 |
| PheGenI | rs1801334 |
| Biobank | rs1801334 |
| 1000 genomes | rs1801334 |
| hgdp | rs1801334 |
| ensembl | rs1801334 |
| geneview | rs1801334 |
| scholar | rs1801334 |
| rs1801334 | |
| pharmgkb | rs1801334 |
| gwascentral | rs1801334 |
| openSNP | rs1801334 |
| 23andMe | rs1801334 |
| SNPshot | rs1801334 |
| SNPdbe | rs1801334 |
| MSV3d | rs1801334 |
| GWAS Ctlg | rs1801334 |
| GMAF | 0.02066 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
[PMID 12975291] Coding polymorphisms in the parkin gene and susceptibility to Parkinson disease.
[PMID 16269266] Geographic and ethnic differences in frequencies of two polymorphisms (D/N394 and L/I272) of the parkin gene in sporadic Parkinson's disease.
| ClinVar | |
|---|---|
| Risk | rs1801334(A;A) |
| Alt | rs1801334(A;A) |
| Reference | Rs1801334(G;G) |
| Significance | Non-pathogenic |
| Disease | Parkinson disease 2 not specified |
| Variation | info |
| Gene | PARK2 |
| CLNDBN | Parkinson disease 2 not specified |
| Reversed | 1 |
| HGVS | NC_000006.11:g.161781225C>T |
| CLNSRC | UniProtKB (protein) |
| CLNACC | RCV000034121.2, RCV000244341.1, |
