| Disease associated variation - ClinVar | | Allele ID | Type | Name | RS#dbSNP | Phenotype IDs | Chromosome | Start | Stop | Reference | Alternate |
|---|
| 167223 | deletion | NC_000016.10:g.31209548_31215370del5823 | -1 | Human Phenotype Ontology:HP:0001518,MedGen:C0024032 | 16 | 31209548 | 31215370 | na | na | | 167223 | deletion | NC_000016.10:g.31209548_31215370del5823 | -1 | Human Phenotype Ontology:HP:0001518,MedGen:C0024032 | 16 | 31220869 | 31226691 | na | na | |