rs17606561, ELOVL2

N. diseases: 2
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 1.000 0.040 6 10982126 3 prime UTR variant G/A snv 0.17 0.800 1.000 2 2011 2012
Autism Spectrum Disorders
CUI: C1510586
Disease: Autism Spectrum Disorders
331 1.000 0.040 6 10982126 3 prime UTR variant G/A snv 0.17 0.010 1.000 1 2018 2018