rs368435864, POLG

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.
Alpers Syndrome (disorder)
CUI: C0205710
Disease: Alpers Syndrome (disorder)
128 1.000 0.080 15 89318736 missense variant C/A;T snv 1.2E-05; 2.0E-05 0.800 1.000 7 2004 2014
Seizures
CUI: C0036572
Disease: Seizures
553 1.000 0.080 15 89318736 missense variant C/A;T snv 1.2E-05; 2.0E-05 0.700 1.000 9 2006 2013