rs704180, ABCC9

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.
Hippocampal sclerosis
CUI: C1504404
Disease: Hippocampal sclerosis
14 0.807 0.240 12 21841177 intron variant A/G snv 0.55 0.030 1.000 3 2015 2017
Alzheimer's Disease
CUI: C0002395
Disease: Alzheimer's Disease
1843 0.807 0.240 12 21841177 intron variant A/G snv 0.55 0.020 1.000 2 2016 2017
Arteriolosclerosis
CUI: C0878486
Disease: Arteriolosclerosis
2 0.807 0.240 12 21841177 intron variant A/G snv 0.55 0.010 1.000 1 2017 2017
Brain atrophy
CUI: C4551584
Disease: Brain atrophy
46 0.807 0.240 12 21841177 intron variant A/G snv 0.55 0.010 1.000 1 2016 2016
Cerebral atrophy
CUI: C0235946
Disease: Cerebral atrophy
44 0.807 0.240 12 21841177 intron variant A/G snv 0.55 0.010 1.000 1 2016 2016
SPHEROCYTOSIS, TYPE 1 (disorder)
CUI: C2674218
Disease: SPHEROCYTOSIS, TYPE 1 (disorder)
16 0.807 0.240 12 21841177 intron variant A/G snv 0.55 0.010 1.000 1 2016 2016