rs866096259
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs866096259(A;A) |
| Make rs866096259(A;C) |
| Make rs866096259(C;C) |
| Reference | GRCh38.p7 38.3/151 |
| Chromosome | 3 |
| Position | 113400632 |
| Gene | CFAP44 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs866096259 |
| dbSNP (classic) | rs866096259 |
| ClinGen | rs866096259 |
| ebi | rs866096259 |
| HLI | rs866096259 |
| Exac | rs866096259 |
| Gnomad | rs866096259 |
| Varsome | rs866096259 |
| LitVar | rs866096259 |
| Map | rs866096259 |
| PheGenI | rs866096259 |
| Biobank | rs866096259 |
| 1000 genomes | rs866096259 |
| hgdp | rs866096259 |
| ensembl | rs866096259 |
| geneview | rs866096259 |
| scholar | rs866096259 |
| rs866096259 | |
| pharmgkb | rs866096259 |
| gwascentral | rs866096259 |
| openSNP | rs866096259 |
| 23andMe | rs866096259 |
| SNPshot | rs866096259 |
| SNPdbe | rs866096259 |
| MSV3d | rs866096259 |
| GWAS Ctlg | rs866096259 |
| Max Magnitude | 0 |
aka NM_001164496.1(CFAP44):c.1387G>T or (p.Glu463Ter)
OMIM pathogenic variant
