rs2236212, 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 10994782 intron variant G/C snv 0.39 0.700 1.000 1 2011 2011
Non-alcoholic Fatty Liver Disease
CUI: C0400966
Disease: Non-alcoholic Fatty Liver Disease
222 1.000 0.040 6 10994782 intron variant G/C snv 0.39 0.010 1.000 1 2019 2019