rs376788209
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs376788209(A;A) |
| Make rs376788209(A;G) |
| Make rs376788209(G;G) |
| Reference | GRCh38.p7 38.3/151 |
| Chromosome | 10 |
| Position | 104230656 |
| Gene | CFAP43 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs376788209 |
| dbSNP (classic) | rs376788209 |
| ClinGen | rs376788209 |
| ebi | rs376788209 |
| HLI | rs376788209 |
| Exac | rs376788209 |
| Gnomad | rs376788209 |
| Varsome | rs376788209 |
| LitVar | rs376788209 |
| Map | rs376788209 |
| PheGenI | rs376788209 |
| Biobank | rs376788209 |
| 1000 genomes | rs376788209 |
| hgdp | rs376788209 |
| ensembl | rs376788209 |
| geneview | rs376788209 |
| scholar | rs376788209 |
| rs376788209 | |
| pharmgkb | rs376788209 |
| gwascentral | rs376788209 |
| openSNP | rs376788209 |
| 23andMe | rs376788209 |
| SNPshot | rs376788209 |
| SNPdbe | rs376788209 |
| MSV3d | rs376788209 |
| GWAS Ctlg | rs376788209 |
| Max Magnitude | 0 |
aka NM_025145.6(CFAP43):c.253C>T or (p.Arg85Trp)
OMIM pathogenic variant
