Disease associated variation - ClinVar Allele ID Type Name RS#dbSNP Phenotype IDs Chromosome Start Stop Reference Alternate 132633 single nucleotide variant NM_005356.4(LCK):c.1022T>C (p.Leu341Pro) 587777335 MedGen:CN186319,OMIM:615758 1 32745329 32745329 T C 132633 single nucleotide variant NM_005356.4(LCK):c.1022T>C (p.Leu341Pro) 587777335 MedGen:CN186319,OMIM:615758 1 32279728 32279728 T C

Disease associated variation - GWAS Central Study Name Source Marker Accession Chromosome Marker Start Marker Stop Alleles Gene Section P-value -log(p-value) GWAS of prostate cancer rs695161 1 32743866 32743866 intronic 0.828372 0.0817745892220986

Disease associated variation - OMIM Ensembl_gene_ID Approved Gene Symbol MIM Number ENSG00000182866.16 LCK 153390