rs864309650, CHCHD2

N. diseases: 4
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 22, AUTOSOMAL DOMINANT
CUI: C4225238
Disease: PARKINSON DISEASE 22, AUTOSOMAL DOMINANT
3 0.851 0.040 7 56104344 missense variant G/A snv 0.800 1.000 1 2015 2015
Parkinson Disease
CUI: C0030567
Disease: Parkinson Disease
990 0.851 0.040 7 56104344 missense variant G/A snv 0.030 1.000 3 2017 2019
Essential Tremor
CUI: C0270736
Disease: Essential Tremor
79 0.851 0.040 7 56104344 missense variant G/A snv 0.010 1.000 1 2017 2017
Parkinson Disease, Familial, Type 1
CUI: C3489791
Disease: Parkinson Disease, Familial, Type 1
27 0.851 0.040 7 56104344 missense variant G/A snv 0.010 1.000 1 2019 2019