rs3798719, ELOVL2

N. diseases: 1
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 6 11036592 intron variant C/T snv 0.18 0.700 1.000 1 2011 2011