Disease associated variation - ClinVar Allele ID Type Name RS#dbSNP Phenotype IDs Chromosome Start Stop Reference Alternate 223036 single nucleotide variant NM_032854.3(CORO6):c.1348G>A (p.Val450Met) 772136445 MedGen:C1527349 17 27942821 27942821 C T 223036 single nucleotide variant NM_032854.3(CORO6):c.1348G>A (p.Val450Met) 772136445 MedGen:C1527349 17 29615803 29615803 C T