rs786205520
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in clinvar |
| Make rs786205520(C;C) |
| Make rs786205520(C;G) |
| Reference | GRCh38.p2 38.2/146 |
| Chromosome | 19 |
| Position | 46755483 |
| Gene | FKRP |
| is a | snp |
| is | mentioned by |
| dbSNP | rs786205520 |
| dbSNP (classic) | rs786205520 |
| ClinGen | rs786205520 |
| ebi | rs786205520 |
| HLI | rs786205520 |
| Exac | rs786205520 |
| Gnomad | rs786205520 |
| Varsome | rs786205520 |
| LitVar | rs786205520 |
| Map | rs786205520 |
| PheGenI | rs786205520 |
| Biobank | rs786205520 |
| 1000 genomes | rs786205520 |
| hgdp | rs786205520 |
| ensembl | rs786205520 |
| geneview | rs786205520 |
| scholar | rs786205520 |
| rs786205520 | |
| pharmgkb | rs786205520 |
| gwascentral | rs786205520 |
| openSNP | rs786205520 |
| 23andMe | rs786205520 |
| SNPshot | rs786205520 |
| SNPdbe | rs786205520 |
| MSV3d | rs786205520 |
| GWAS Ctlg | rs786205520 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs786205520(C;C) |
| Alt | rs786205520(C;C) |
| Reference | Rs786205520(G;G) |
| Significance | Probable-non-pathogenic |
| Disease | not specified |
| Variation | info |
| Gene | FKRP |
| CLNDBN | not specified |
| Reversed | 0 |
| HGVS | NC_000019.9:g.47258740G>C |
| CLNSRC | |
| CLNACC | RCV000171285.2, |
