rs1382597320, ATN1

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.
Parkinson Disease
CUI: C0030567
Disease: Parkinson Disease
990 0.882 0.160 12 6934305 missense variant A/G snv 7.0E-06 0.020 1.000 2 2008 2019
Amyotrophic Lateral Sclerosis, Familial
CUI: C4551993
Disease: Amyotrophic Lateral Sclerosis, Familial
68 0.882 0.160 12 6934305 missense variant A/G snv 7.0E-06 0.010 1.000 1 2008 2008
Huntington Disease
CUI: C0020179
Disease: Huntington Disease
115 0.882 0.160 12 6934305 missense variant A/G snv 7.0E-06 0.010 1.000 1 2008 2008