rs765256758
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs765256758(C;C) |
| Make rs765256758(C;T) |
| Make rs765256758(T;T) |
| Reference | GRCh38.p7 38.3/151 |
| Chromosome | 3 |
| Position | 190402428 |
| Gene | CLDN16 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs765256758 |
| dbSNP (classic) | rs765256758 |
| ClinGen | rs765256758 |
| ebi | rs765256758 |
| HLI | rs765256758 |
| Exac | rs765256758 |
| Gnomad | rs765256758 |
| Varsome | rs765256758 |
| LitVar | rs765256758 |
| Map | rs765256758 |
| PheGenI | rs765256758 |
| Biobank | rs765256758 |
| 1000 genomes | rs765256758 |
| hgdp | rs765256758 |
| ensembl | rs765256758 |
| geneview | rs765256758 |
| scholar | rs765256758 |
| rs765256758 | |
| pharmgkb | rs765256758 |
| gwascentral | rs765256758 |
| openSNP | rs765256758 |
| 23andMe | rs765256758 |
| SNPshot | rs765256758 |
| SNPdbe | rs765256758 |
| MSV3d | rs765256758 |
| GWAS Ctlg | rs765256758 |
| Max Magnitude | 0 |
aka NM_006580.3(CLDN16):c.416C>T or (p.Ala139Val)
OMIM pathogenic variant
