Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs1000778
rs1000778
FADS3
1.000 0.040 11 61887833 intron variant A/G snv 0.59
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement 		0.700 1.000 1 2011 2011
dbSNP: rs1000778
rs1000778
FADS3
1.000 0.040 11 61887833 intron variant A/G snv 0.59
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012
dbSNP: rs1000778
rs1000778
FADS3
1.000 0.040 11 61887833 intron variant A/G snv 0.59
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		0.010 1.000 1 2017 2017