rs79524815, HDAC9

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.
Cerebral Amyloid Angiopathy
CUI: C0085220
Disease: Cerebral Amyloid Angiopathy
22 0.851 0.240 7 18658708 intron variant T/G snv 3.8E-02 0.700 1.000 1 2018 2018
Alzheimer's Disease
CUI: C0002395
Disease: Alzheimer's Disease
1843 0.851 0.240 7 18658708 intron variant T/G snv 3.8E-02 0.010 1.000 1 2018 2018
AURAL ATRESIA, CONGENITAL
CUI: C1842937
Disease: AURAL ATRESIA, CONGENITAL
29 0.851 0.240 7 18658708 intron variant T/G snv 3.8E-02 0.010 1.000 1 2018 2018
Senile Plaques
CUI: C0333463
Disease: Senile Plaques
21 0.851 0.240 7 18658708 intron variant T/G snv 3.8E-02 0.010 1.000 1 2018 2018