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
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
rs4246215
FADS2 ; FEN1
0.677 0.320 11 61796827 3 prime UTR variant G/C;T snv 6
rs174583
FADS2
0.807 0.320 11 61842278 intron variant C/T snv 0.35 5
rs2851682
FADS2
11 61848540 intron variant A/G snv 9.9E-02 5
rs174541
FADS2
1.000 0.080 11 61798436 intron variant T/C snv 0.29 4
rs174556
FADS2 ; FADS1
0.925 0.160 11 61813163 intron variant C/T snv 0.26 3
rs968567
FADS2 ; FADS1
0.851 0.240 11 61828092 intron variant C/T snv 0.11 3
rs17156426
FADS2
11 61841851 intron variant A/G;T snv 2
rs17156442
FADS2
11 61846551 intron variant C/T snv 0.11 2
rs174574
FADS2
1.000 0.080 11 61832870 intron variant A/C snv 0.55 2
rs174575
FADS2
1.000 0.040 11 61834531 intron variant C/G snv 0.25 2
rs174579
FADS2
11 61838141 intron variant C/T snv 0.16 2
rs174585
FADS2
11 61844222 intron variant G/A;T snv 2
rs174591
FADS2
11 61850204 intron variant T/A;G snv 2
rs174593
FADS2
11 61851359 intron variant T/C snv 0.24 2
rs174597
FADS2
11 61853568 intron variant G/A;C;T snv 2
rs174602
FADS2
1.000 0.080 11 61856942 non coding transcript exon variant T/C snv 0.37 2
rs174605
FADS2
11 61859449 intron variant G/T snv 0.20 2
rs174611
FADS2
11 61860409 intron variant T/C snv 0.21 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