Disease associated variation - ClinVar | Allele ID | Type | Name | RS#dbSNP | Phenotype IDs | Chromosome | Start | Stop | Reference | Alternate | 362049 | deletion | NM_014957.2(DENND3):c.1920delG (p.Lys640Asnfs) | -1 | MedGen:C2931876,OMIM:142623 | 8 | 142178509 | 142178509 | G | - | 362049 | deletion | NM_014957.2(DENND3):c.1920delG (p.Lys640Asnfs) | -1 | MedGen:C2931876,OMIM:142623 | 8 | 141168410 | 141168410 | G | - | |