rs760609580
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs760609580(A;A) |
| Make rs760609580(A;G) |
| Make rs760609580(G;G) |
| Reference | GRCh38.p7 38.3/151 |
| Chromosome | 10 |
| Position | 104162023 |
| Gene | CFAP43 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs760609580 |
| dbSNP (classic) | rs760609580 |
| ClinGen | rs760609580 |
| ebi | rs760609580 |
| HLI | rs760609580 |
| Exac | rs760609580 |
| Gnomad | rs760609580 |
| Varsome | rs760609580 |
| LitVar | rs760609580 |
| Map | rs760609580 |
| PheGenI | rs760609580 |
| Biobank | rs760609580 |
| 1000 genomes | rs760609580 |
| hgdp | rs760609580 |
| ensembl | rs760609580 |
| geneview | rs760609580 |
| scholar | rs760609580 |
| rs760609580 | |
| pharmgkb | rs760609580 |
| gwascentral | rs760609580 |
| openSNP | rs760609580 |
| 23andMe | rs760609580 |
| SNPshot | rs760609580 |
| SNPdbe | rs760609580 |
| MSV3d | rs760609580 |
| GWAS Ctlg | rs760609580 |
| Max Magnitude | 0 |
aka NM_025145.6(CFAP43):c.3352C>T or (p.Arg1118Ter)
OMIM pathogenic variant
