rs780798708
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs780798708(-;-) |
| Make rs780798708(-;AT) |
| Make rs780798708(AT;AT) |
| Reference | GRCh38.p7 38.3/151 |
| Chromosome | 3 |
| Position | 113380945 |
| Gene | CFAP44 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs780798708 |
| dbSNP (classic) | rs780798708 |
| ClinGen | rs780798708 |
| ebi | rs780798708 |
| HLI | rs780798708 |
| Exac | rs780798708 |
| Gnomad | rs780798708 |
| Varsome | rs780798708 |
| LitVar | rs780798708 |
| Map | rs780798708 |
| PheGenI | rs780798708 |
| Biobank | rs780798708 |
| 1000 genomes | rs780798708 |
| hgdp | rs780798708 |
| ensembl | rs780798708 |
| geneview | rs780798708 |
| scholar | rs780798708 |
| rs780798708 | |
| pharmgkb | rs780798708 |
| gwascentral | rs780798708 |
| openSNP | rs780798708 |
| 23andMe | rs780798708 |
| SNPshot | rs780798708 |
| SNPdbe | rs780798708 |
| MSV3d | rs780798708 |
| GWAS Ctlg | rs780798708 |
| Max Magnitude | 0 |
aka NM_018338.3(CFAP44):c.2005_2006delAT or (p.Met669Valfs)
OMIM pathogenic variant
