rs3756963, ELOVL2

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.
Phospholipid measurement
CUI: C0202177
Disease: Phospholipid measurement
306 0.882 0.200 6 11021921 intron variant T/C snv 0.24 0.700 1.000 1 2011 2011
Acute Chest Syndrome
CUI: C0742343
Disease: Acute Chest Syndrome
135 0.882 0.200 6 11021921 intron variant T/C snv 0.24 0.010 1.000 1 2013 2013
Autism Spectrum Disorders
CUI: C1510586
Disease: Autism Spectrum Disorders
331 0.882 0.200 6 11021921 intron variant T/C snv 0.24 0.010 1.000 1 2018 2018
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 0.882 0.200 6 11021921 intron variant T/C snv 0.24 0.010 1.000 1 2011 2011