rs10498676, ELOVL2

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.
Autism Spectrum Disorders
CUI: C1510586
Disease: Autism Spectrum Disorders
331 0.925 0.040 6 11026766 intron variant G/A snv 0.18 0.010 1.000 1 2018 2018
Autistic Disorder
CUI: C0004352
Disease: Autistic Disorder
395 0.925 0.040 6 11026766 intron variant G/A snv 0.18 0.010 1.000 1 2018 2018
Phospholipid measurement
CUI: C0202177
Disease: Phospholipid measurement
306 0.925 0.040 6 11026766 intron variant G/A snv 0.18 0.700 1.000 1 2011 2011