rs2267369
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in clinvar |
| Make rs2267369(C;T) |
| Make rs2267369(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 22 |
| Position | 38169340 |
| Gene | PLA2G6 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs2267369 |
| dbSNP (classic) | rs2267369 |
| ClinGen | rs2267369 |
| ebi | rs2267369 |
| HLI | rs2267369 |
| Exac | rs2267369 |
| Gnomad | rs2267369 |
| Varsome | rs2267369 |
| LitVar | rs2267369 |
| Map | rs2267369 |
| PheGenI | rs2267369 |
| Biobank | rs2267369 |
| 1000 genomes | rs2267369 |
| hgdp | rs2267369 |
| ensembl | rs2267369 |
| geneview | rs2267369 |
| scholar | rs2267369 |
| rs2267369 | |
| pharmgkb | rs2267369 |
| gwascentral | rs2267369 |
| openSNP | rs2267369 |
| 23andMe | rs2267369 |
| SNPshot | rs2267369 |
| SNPdbe | rs2267369 |
| MSV3d | rs2267369 |
| GWAS Ctlg | rs2267369 |
| GMAF | 0.0753 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 22459563] Association between PLA2G6 gene polymorphisms and Parkinson's disease in the Chinese Han population
| ClinVar | |
|---|---|
| Risk | rs2267369(T;T) |
| Alt | rs2267369(T;T) |
| Reference | Rs2267369(C;C) |
| Significance | Probable-non-pathogenic |
| Disease | not specified Infantile neuroaxonal dystrophy |
| Variation | info |
| Gene | PLA2G6 |
| CLNDBN | not specified Infantile neuroaxonal dystrophy |
| Reversed | 0 |
| HGVS | NC_000022.10:g.38565347C>T |
| CLNSRC | ClinVar University of Chicago |
| CLNACC | RCV000147337.1, RCV000299100.1, |
