SLFN12, schlafen family member 12, 55106

N. diseases: 14; N. variants: 0
Disease: Sezary Syndrome ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0036920
Disease: Sezary Syndrome
Sezary Syndrome 		0.010 GeneticVariation disease BEFREE Novel TBL1XR1, EPHA7 and SLFN12 mutations in a Sezary syndrome patient discovered by whole exome sequencing. 24689486 2014