Source: FB:FBal0326927
Genes: Chchd2 (Dme)
Synonyms: Not Available
Variant Type: deletion
Molecular Consequence: stop_lost, 3_prime_UTR_variant, splice_donor_variant, splice_acceptor_variant, intron_variant
Diseases: frontotemporal dementia and/or amyotrophic lateral sclerosis 2, Parkinson's disease, Parkinson's disease 22
Variant Name: Not Available