Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs2391388
rs2391388
1 95020269 intron variant A/C snv 0.49
CUI: C1281901
Disease: Fatty acid measurement
Fatty acid measurement
0.700 1.000 1 2013 2013
dbSNP: rs6675668
rs6675668
1 95050081 intron variant T/G snv 0.43
CUI: C1281901
Disease: Fatty acid measurement
Fatty acid measurement
0.700 1.000 1 2013 2013