rs368497893
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in clinvar |
| Make rs368497893(C;T) |
| Make rs368497893(T;T) |
| Reference | GRCh38.p7 38.3/149 |
| Chromosome | 22 |
| Position | 38132831 |
| Gene | PLA2G6 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs368497893 |
| dbSNP (classic) | rs368497893 |
| ClinGen | rs368497893 |
| ebi | rs368497893 |
| HLI | rs368497893 |
| Exac | rs368497893 |
| Gnomad | rs368497893 |
| Varsome | rs368497893 |
| LitVar | rs368497893 |
| Map | rs368497893 |
| PheGenI | rs368497893 |
| Biobank | rs368497893 |
| 1000 genomes | rs368497893 |
| hgdp | rs368497893 |
| ensembl | rs368497893 |
| geneview | rs368497893 |
| scholar | rs368497893 |
| rs368497893 | |
| pharmgkb | rs368497893 |
| gwascentral | rs368497893 |
| openSNP | rs368497893 |
| 23andMe | rs368497893 |
| SNPshot | rs368497893 |
| SNPdbe | rs368497893 |
| MSV3d | rs368497893 |
| GWAS Ctlg | rs368497893 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs368497893(T;T) |
| Alt | rs368497893(T;T) |
| Reference | Rs368497893(C;C) |
| Significance | Pathogenic |
| Disease | not provided |
| Variation | info |
| Gene | PLA2G6 |
| CLNDBN | not provided |
| Reversed | 0 |
| HGVS | NC_000022.10:g.38528838C>T |
| CLNSRC | |
| CLNACC | RCV000266508.1, |
