rs762760856
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs762760856(A;A) |
| Make rs762760856(A;T) |
| Make rs762760856(T;T) |
| Reference | GRCh38.p7 38.3/151 |
| Chromosome | 3 |
| Position | 113396528 |
| Gene | CFAP44 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs762760856 |
| dbSNP (classic) | rs762760856 |
| ClinGen | rs762760856 |
| ebi | rs762760856 |
| HLI | rs762760856 |
| Exac | rs762760856 |
| Gnomad | rs762760856 |
| Varsome | rs762760856 |
| LitVar | rs762760856 |
| Map | rs762760856 |
| PheGenI | rs762760856 |
| Biobank | rs762760856 |
| 1000 genomes | rs762760856 |
| hgdp | rs762760856 |
| ensembl | rs762760856 |
| geneview | rs762760856 |
| scholar | rs762760856 |
| rs762760856 | |
| pharmgkb | rs762760856 |
| gwascentral | rs762760856 |
| openSNP | rs762760856 |
| 23andMe | rs762760856 |
| SNPshot | rs762760856 |
| SNPdbe | rs762760856 |
| MSV3d | rs762760856 |
| GWAS Ctlg | rs762760856 |
| Max Magnitude | 0 |
aka NM_001164496.1(CFAP44):c.1769T>A or (p.Leu590Gln)
OMIM pathogenic variant
