rs369751362
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in clinvar |
| Make rs369751362(C;T) |
| Make rs369751362(T;T) |
| Reference | GRCh38.p2 38.2/147 |
| Chromosome | 16 |
| Position | 15720895 |
| Gene | MYH11, NDE1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs369751362 |
| dbSNP (classic) | rs369751362 |
| ClinGen | rs369751362 |
| ebi | rs369751362 |
| HLI | rs369751362 |
| Exac | rs369751362 |
| Gnomad | rs369751362 |
| Varsome | rs369751362 |
| LitVar | rs369751362 |
| Map | rs369751362 |
| PheGenI | rs369751362 |
| Biobank | rs369751362 |
| 1000 genomes | rs369751362 |
| hgdp | rs369751362 |
| ensembl | rs369751362 |
| geneview | rs369751362 |
| scholar | rs369751362 |
| rs369751362 | |
| pharmgkb | rs369751362 |
| gwascentral | rs369751362 |
| openSNP | rs369751362 |
| 23andMe | rs369751362 |
| SNPshot | rs369751362 |
| SNPdbe | rs369751362 |
| MSV3d | rs369751362 |
| GWAS Ctlg | rs369751362 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs369751362(T;T) |
| Alt | rs369751362(T;T) |
| Reference | Rs369751362(C;C) |
| Significance | Probable-Pathogenic |
| Disease | not specified |
| Variation | info |
| Gene | NDE1 MYH11 |
| CLNDBN | not specified |
| Reversed | 0 |
| HGVS | NC_000016.9:g.15814752C>T |
| CLNSRC | |
| CLNACC | RCV000182523.3, |
