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.
Epilepsy, Generalized
CUI: C0014548
Disease: Epilepsy, Generalized
36 0.882 0.160 15 89327329 frameshift variant AG/- delins 4.0E-06 1.4E-05 0.700 1.000 2 2003 2008
Obesity
CUI: C0028754
Disease: Obesity
1111 0.882 0.160 15 89327329 frameshift variant AG/- delins 4.0E-06 1.4E-05 0.700 1.000 2 2003 2008
Alpers Syndrome (disorder)
CUI: C0205710
Disease: Alpers Syndrome (disorder)
128 0.882 0.160 15 89327329 frameshift variant AG/- delins 4.0E-06 1.4E-05 0.700 1.000 1 2003 2003