Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs174547
FADS2 ; FADS1
0.742 0.240 11 61803311 intron variant T/C snv 0.28 10
rs174546
FADS1 ; FADS2
0.807 0.200 11 61802358 3 prime UTR variant C/T snv 0.28 9
rs174548
FADS2 ; FADS1
0.851 0.160 11 61803876 5 prime UTR variant C/G;T snv 9
rs174550
FADS1 ; FADS2
0.925 0.160 11 61804006 5 prime UTR variant T/C snv 0.28 6
rs968567
FADS2 ; FADS1
0.851 0.240 11 61828092 intron variant C/T snv 0.11 3
rs174549
FADS2 ; FADS1
0.851 0.240 11 61803910 5 prime UTR variant G/A snv 0.26 3
rs174556
FADS2 ; FADS1
0.925 0.160 11 61813163 intron variant C/T snv 0.26 3
rs174554
FADS1 ; FADS2
1.000 0.080 11 61811991 intron variant A/G snv 0.40 0.28 1
rs99780
FADS1 ; FADS2
1.000 0.080 11 61829161 intron variant C/T snv 0.38 1
rs174560
FADS1 ; FADS2
1.000 0.080 11 61814292 non coding transcript exon variant T/C snv 0.30 1
rs174553
FADS1 ; FADS2
1.000 0.040 11 61807686 intron variant A/G;T snv 0.28 1
rs174559
FADS1 ; FADS2
11 61814184 non coding transcript exon variant G/A snv 0.23 1
rs174566
FADS1 ; FADS2
0.925 0.160 11 61824890 intron variant A/G snv 0.34 1
rs174568
FADS1 ; FADS2
1.000 0.080 11 61826344 missense variant C/A;T snv 0.37 1
rs61897792
FADS1 ; FADS2
11 61819414 intron variant C/T snv 7.1E-02 1
rs174545
FADS1 ; FADS2
1.000 0.080 11 61801834 3 prime UTR variant C/A;G snv 0.28 1
rs174544
FADS1 ; FADS2
11 61800281 3 prime UTR variant C/A snv 0.25 1
rs174555
FADS2 ; FADS1
11 61812288 intron variant T/C snv 0.26 1
rs174562
FADS2 ; FADS1
1.000 0.080 11 61817672 intron variant A/G snv 0.28 1
rs174561
MIR1908 ; FADS1 ; FADS2
1.000 0.080 11 61815236 5 prime UTR variant T/C snv 0.31 0.26 1