rs6787362
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs6787362(A;A) |
| Make rs6787362(A;G) |
| Make rs6787362(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 3 |
| Position | 69178228 |
| Gene | FRMD4B |
| is a | snp |
| is | mentioned by |
| dbSNP | rs6787362 |
| dbSNP (classic) | rs6787362 |
| ClinGen | rs6787362 |
| ebi | rs6787362 |
| HLI | rs6787362 |
| Exac | rs6787362 |
| Gnomad | rs6787362 |
| Varsome | rs6787362 |
| LitVar | rs6787362 |
| Map | rs6787362 |
| PheGenI | rs6787362 |
| Biobank | rs6787362 |
| 1000 genomes | rs6787362 |
| hgdp | rs6787362 |
| ensembl | rs6787362 |
| geneview | rs6787362 |
| scholar | rs6787362 |
| rs6787362 | |
| pharmgkb | rs6787362 |
| gwascentral | rs6787362 |
| openSNP | rs6787362 |
| 23andMe | rs6787362 |
| SNPshot | rs6787362 |
| SNPdbe | rs6787362 |
| MSV3d | rs6787362 |
| GWAS Ctlg | rs6787362 |
| GMAF | 0.07943 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
[PMID 20124441
] Common variants in HSPB7 and FRMD4B associated with advanced heart failure
[PMID 20718813] Association of An Intronic, but Not Any Exonic, FRMD4B Sequence Variant and Heart Failure
