rs816411, CHCHD2

N. diseases: 3
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.
Amino acids measurement
CUI: C0201874
Disease: Amino acids measurement
92 1.000 0.040 7 56103796 intron variant C/T snv 0.53 0.700 1.000 1 2019 2019
Serine measurement
CUI: C0523888
Disease: Serine measurement
18 1.000 0.040 7 56103796 intron variant C/T snv 0.53 0.700 1.000 1 2019 2019
Parkinson Disease
CUI: C0030567
Disease: Parkinson Disease
990 1.000 0.040 7 56103796 intron variant C/T snv 0.53 0.010 1 2015 2015