rs2306604, TFAM

N. diseases: 5
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.
Parkinson Disease
CUI: C0030567
Disease: Parkinson Disease
990 0.827 0.080 10 58388932 intron variant A/C;G;T snv 0.030 1.000 3 2007 2013
Alzheimer's Disease
CUI: C0002395
Disease: Alzheimer's Disease
1843 0.827 0.080 10 58388932 intron variant A/C;G;T snv 0.010 1 2013 2013
Dementia
CUI: C0497327
Disease: Dementia
176 0.827 0.080 10 58388932 intron variant A/C;G;T snv 0.010 1 2013 2013
Lewy Body Disease
CUI: C0752347
Disease: Lewy Body Disease
41 0.827 0.080 10 58388932 intron variant A/C;G;T snv 0.010 1.000 1 2013 2013
Presenile dementia
CUI: C0011265
Disease: Presenile dementia
159 0.827 0.080 10 58388932 intron variant A/C;G;T snv 0.010 1 2013 2013