rs142444896, CHCHD2

N. diseases: 6
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.
Alzheimer's Disease
CUI: C0002395
Disease: Alzheimer's Disease
1843 0.807 0.120 7 56106409 missense variant G/A snv 9.3E-03 7.5E-03 0.010 1 2018 2018
Amyotrophic Lateral Sclerosis
CUI: C0002736
Disease: Amyotrophic Lateral Sclerosis
485 0.807 0.120 7 56106409 missense variant G/A snv 9.3E-03 7.5E-03 0.020 0.500 2 2016 2018
Frontotemporal dementia
CUI: C0338451
Disease: Frontotemporal dementia
215 0.807 0.120 7 56106409 missense variant G/A snv 9.3E-03 7.5E-03 0.010 1.000 1 2018 2018
Parkinson Disease
CUI: C0030567
Disease: Parkinson Disease
990 0.807 0.120 7 56106409 missense variant G/A snv 9.3E-03 7.5E-03 0.010 1.000 1 2016 2016
Parkinson Disease, Familial, Type 1
CUI: C3489791
Disease: Parkinson Disease, Familial, Type 1
27 0.807 0.120 7 56106409 missense variant G/A snv 9.3E-03 7.5E-03 0.010 1.000 1 2016 2016
Sporadic Parkinson disease
CUI: C4511452
Disease: Sporadic Parkinson disease
65 0.807 0.120 7 56106409 missense variant G/A snv 9.3E-03 7.5E-03 0.020 1.000 2 2015 2016