rs6675668, ALG14

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.
Fatty acid measurement
CUI: C1281901
Disease: Fatty acid measurement
116 1 95050081 intron variant T/G snv 0.43 0.700 1.000 1 2013 2013
Phospholipid measurement
CUI: C0202177
Disease: Phospholipid measurement
306 1 95050081 intron variant T/G snv 0.43 0.700 1.000 1 2013 2013