Disease associated variation - ClinVar Allele ID Type Name RS#dbSNP Phenotype IDs Chromosome Start Stop Reference Alternate 171530 single nucleotide variant NM_001127585.1(ING4):c.254C>A (p.Ala85Asp) 193921122 MedGen:C0376358,OMIM:176807,SNOMED CT:C0376358 12 6762167 6762167 G T 171530 single nucleotide variant NM_001127585.1(ING4):c.254C>A (p.Ala85Asp) 193921122 MedGen:C0376358,OMIM:176807,SNOMED CT:C0376358 12 6653001 6653001 G T

Disease associated variation - OMIM Ensembl_gene_ID Approved Gene Symbol MIM Number ENSG00000111653.19 ING4 608524