rs756121249
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (T;T) | 0 | common in clinvar |
| Make rs756121249(A;A) |
| Make rs756121249(A;T) |
| Reference | GRCh38.p7 38.3/150 |
| Chromosome | 8 |
| Position | 74350570 |
| Gene | GDAP1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs756121249 |
| dbSNP (classic) | rs756121249 |
| ClinGen | rs756121249 |
| ebi | rs756121249 |
| HLI | rs756121249 |
| Exac | rs756121249 |
| Gnomad | rs756121249 |
| Varsome | rs756121249 |
| LitVar | rs756121249 |
| Map | rs756121249 |
| PheGenI | rs756121249 |
| Biobank | rs756121249 |
| 1000 genomes | rs756121249 |
| hgdp | rs756121249 |
| ensembl | rs756121249 |
| geneview | rs756121249 |
| scholar | rs756121249 |
| rs756121249 | |
| pharmgkb | rs756121249 |
| gwascentral | rs756121249 |
| openSNP | rs756121249 |
| 23andMe | rs756121249 |
| SNPshot | rs756121249 |
| SNPdbe | rs756121249 |
| MSV3d | rs756121249 |
| GWAS Ctlg | rs756121249 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs756121249(A;A) |
| Alt | rs756121249(A;A) |
| Reference | Rs756121249(T;T) |
| Significance | Probable-Pathogenic |
| Disease | not provided |
| Variation | info |
| Gene | GDAP1 |
| CLNDBN | not provided |
| Reversed | 0 |
| HGVS | NC_000008.10:g.75262805T>A |
| CLNSRC | |
| CLNACC | RCV000489068.1, |
