rs768831533
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs768831533(A;A) |
| Make rs768831533(A;G) |
| Make rs768831533(G;G) |
| Reference | GRCh38.p7 38.3/151 |
| Chromosome | 10 |
| Position | 104143452 |
| Gene | CFAP43 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs768831533 |
| dbSNP (classic) | rs768831533 |
| ClinGen | rs768831533 |
| ebi | rs768831533 |
| HLI | rs768831533 |
| Exac | rs768831533 |
| Gnomad | rs768831533 |
| Varsome | rs768831533 |
| LitVar | rs768831533 |
| Map | rs768831533 |
| PheGenI | rs768831533 |
| Biobank | rs768831533 |
| 1000 genomes | rs768831533 |
| hgdp | rs768831533 |
| ensembl | rs768831533 |
| geneview | rs768831533 |
| scholar | rs768831533 |
| rs768831533 | |
| pharmgkb | rs768831533 |
| gwascentral | rs768831533 |
| openSNP | rs768831533 |
| 23andMe | rs768831533 |
| SNPshot | rs768831533 |
| SNPdbe | rs768831533 |
| MSV3d | rs768831533 |
| GWAS Ctlg | rs768831533 |
| Max Magnitude | 0 |
aka NM_025145.6(CFAP43):c.4132C>T or (p.Arg1378Ter)
OMIM pathogenic variant
