rs387906420, TRNF

N. diseases: 2
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
MELAS Syndrome
CUI: C0162671
Disease: MELAS Syndrome
53 0.925 0.200 MT 616 non coding transcript exon variant T/C;G snv 0.700 1.000 1 2010 2010
EPILEPSY, MITOCHONDRIAL
CUI: C4016624
Disease: EPILEPSY, MITOCHONDRIAL
1 0.925 0.200 MT 616 non coding transcript exon variant T/C;G snv 0.700 0