Source: BEFREE

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs6465657
rs6465657
LMTK2
0.807 0.280 7 98187015 intron variant C/T snv 0.41 0.37
CUI: C0019829
Disease: Hodgkin Disease
Hodgkin Disease 		0.010 1.000 1 2011 2011
dbSNP: rs6465657
rs6465657
LMTK2
0.807 0.280 7 98187015 intron variant C/T snv 0.41 0.37
CUI: C0026764
Disease: Multiple Myeloma
Multiple Myeloma 		0.010 1.000 1 2011 2011
dbSNP: rs6465657
rs6465657
LMTK2
0.807 0.280 7 98187015 intron variant C/T snv 0.41 0.37
CUI: C0025202
Disease: melanoma
melanoma 		0.010 1.000 1 2011 2011
dbSNP: rs6465657
rs6465657
LMTK2
0.807 0.280 7 98187015 intron variant C/T snv 0.41 0.37
CUI: C0001418
Disease: Adenocarcinoma
Adenocarcinoma 		0.010 1.000 1 2010 2010