Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1535
FADS2
0.752 0.240 11 61830500 intron variant A/G snv 0.31 10
rs174570
FADS2
0.882 0.200 11 61829740 intron variant C/T snv 0.15 10
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
rs174576
FADS2
0.851 0.200 11 61836038 intron variant C/A;T snv 9
rs174548
FADS2 ; FADS1
0.851 0.160 11 61803876 5 prime UTR variant C/G;T snv 9
rs174601
FADS2
0.925 0.080 11 61855668 non coding transcript exon variant C/A;T snv 8
rs174550
FADS1 ; FADS2
0.925 0.160 11 61804006 5 prime UTR variant T/C snv 0.28 6
rs4246215
FADS2 ; FEN1
0.677 0.320 11 61796827 3 prime UTR variant G/C;T snv 6
rs2851682
FADS2
11 61848540 intron variant A/G snv 9.9E-02 5
rs174583
FADS2
0.807 0.320 11 61842278 intron variant C/T snv 0.35 5
rs174577
FADS2
1.000 0.080 11 61837342 intron variant C/A snv 0.38 5
rs174541
FADS2
1.000 0.080 11 61798436 intron variant T/C snv 0.29 4
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
rs2727270
FADS2
11 61835765 intron variant C/T snv 0.12 2
rs174575
FADS2
1.000 0.040 11 61834531 intron variant C/G snv 0.25 2
rs2727271
FADS2
11 61835886 intron variant A/T snv 0.12 2
rs498793
FADS2
1.000 0.040 11 61857233 intron variant T/C snv 0.62 2
rs174574
FADS2
1.000 0.080 11 61832870 intron variant A/C snv 0.55 2
rs174602
FADS2
1.000 0.080 11 61856942 non coding transcript exon variant T/C snv 0.37 2
rs174616
FADS2
1.000 0.080 11 61861650 intron variant G/A snv 0.51 2
rs17764324
FADS2
11 61867616 downstream gene variant G/A;T snv 2
rs916924
FADS2
11 61851709 intron variant T/C snv 9.1E-02 2