Source: GWASDB

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: rs99780
rs99780
FADS1 ; FADS2
1.000 0.080 11 61829161 intron variant C/T snv 0.38
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012
dbSNP: rs174553
rs174553
FADS1 ; FADS2
1.000 0.040 11 61807686 intron variant A/G;T snv 0.28
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012
dbSNP: rs174555
rs174555
FADS1 ; FADS2
11 61812288 intron variant T/C snv 0.26
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 2 2012 2013
dbSNP: rs174544
rs174544
FADS1 ; FADS2
11 61800281 3 prime UTR variant C/A snv 0.25
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012
dbSNP: rs174559
rs174559
FADS1 ; FADS2
11 61814184 non coding transcript exon variant G/A snv 0.23
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012
dbSNP: rs61897792
rs61897792
FADS1 ; FADS2
11 61819414 intron variant C/T snv 7.1E-02
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012