rs750428882, TPP1

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.
Seizures
CUI: C0036572
Disease: Seizures
553 1.000 0.120 11 6616375 missense variant G/A;C snv 4.0E-06 0.700 1.000 4 2009 2013
Neuronal Ceroid-Lipofuscinoses
CUI: C0027877
Disease: Neuronal Ceroid-Lipofuscinoses
74 1.000 0.120 11 6616375 missense variant G/A;C snv 4.0E-06 0.700 0