CLDN19
From SNPedia
| is a | gene |
| is | mentioned by |
| Full name | claudin 19 |
| EntrezGene | 149461 |
| PheGenI | 149461 |
| VariationViewer | 149461 |
| ClinVar | CLDN19 |
| GeneCards | CLDN19 |
| dbSNP | 149461 |
| Diseases | CLDN19 |
| SADR | 149461 |
| HugeNav | 149461 |
| wikipedia | CLDN19 |
| CLDN19 | |
| gopubmed | CLDN19 |
| EVS | CLDN19 |
| HEFalMp | CLDN19 |
| MyGene2 | CLDN19 |
| 23andMe | CLDN19 |
| UniProt | Q8N6F1 |
| Ensembl | ENSG00000164007 |
| OMIM | 610036 |
| # SNPs | 3 |
| Max Magnitude | Chromosome position | Summary | |
|---|---|---|---|
| rs118203979 | 0 | 42,740,005 | |
| rs118203980 | 0 | 42,739,895 | |
| rs118203981 | 0 | 42,738,540 |
Associated with hypomagnesemia.
