rs7225002, KANSL1

N. diseases: 7
Source: INFERRED ×
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
0.925 0.080 17 46111701 intron variant A/G snv 0.39 0.700 1.000 3 2009 2012
Corpuscular Hemoglobin Concentration Mean
CUI: C4528257
Disease: Corpuscular Hemoglobin Concentration Mean
0.925 0.080 17 46111701 intron variant A/G snv 0.39 0.700 1.000 1 2012 2012
Finding of Mean Corpuscular Hemoglobin
CUI: C1261502
Disease: Finding of Mean Corpuscular Hemoglobin
0.925 0.080 17 46111701 intron variant A/G snv 0.39 0.700 1.000 1 2019 2019
Major Depressive Disorder
CUI: C1269683
Disease: Major Depressive Disorder
0.925 0.080 17 46111701 intron variant A/G snv 0.39 0.700 1.000 1 2018 2018
Mood Disorders
CUI: C0525045
Disease: Mood Disorders
0.925 0.080 17 46111701 intron variant A/G snv 0.39 0.700 1.000 1 2018 2018
RDW - Red blood cell distribution width result
CUI: C1304746
Disease: RDW - Red blood cell distribution width result
0.925 0.080 17 46111701 intron variant A/G snv 0.39 0.700 1.000 1 2019 2019
Red cell distribution width determination
CUI: C0427460
Disease: Red cell distribution width determination
0.925 0.080 17 46111701 intron variant A/G snv 0.39 0.700 1.000 1 2019 2019