Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs603424
PKD2L1
1.000 0.080 10 100315722 intron variant G/A snv 0.34 13
rs174541
FADS2
1.000 0.080 11 61798436 intron variant T/C snv 0.29 8
rs4775041
ALDH1A2
1.000 0.040 15 58382496 intron variant G/C snv 0.24 8
rs174574
FADS2
1.000 0.080 11 61832870 intron variant A/C snv 0.55 7
rs174455
FADS3
1.000 0.080 11 61888645 intron variant G/A;C snv 5
rs174528
TMEM258 ; MYRF
1.000 0.080 11 61776027 intron variant T/C snv 0.42 0.42 5
rs2072114
FADS2
1.000 0.080 11 61837743 intron variant A/G snv 0.19 0.16 4
rs1000778
FADS3
1.000 0.040 11 61887833 intron variant A/G snv 0.59 3
rs1077989
GPHN ; TMEM229B
1.000 0.080 14 67509105 intron variant A/C snv 0.39 3
rs174448 1.000 0.120 11 61872101 downstream gene variant G/A snv 0.61 3
rs174450
FADS3
1.000 0.080 11 61874070 intron variant G/T snv 0.44 3
rs174534
MYRF ; TMEM258
1.000 0.080 11 61781986 non coding transcript exon variant A/G snv 0.28 3
rs174575
FADS2
1.000 0.040 11 61834531 intron variant C/G snv 0.25 3
rs174602
FADS2
1.000 0.080 11 61856942 non coding transcript exon variant T/C snv 0.37 3
rs174616
FADS2
1.000 0.080 11 61861650 intron variant G/A snv 0.51 3
rs2845573
FADS2
1.000 0.040 11 61834436 intron variant A/G snv 9.7E-02 3
rs498793
FADS2
1.000 0.040 11 61857233 intron variant T/C snv 0.62 3
rs526126
FADS2
1.000 0.040 11 61857413 intron variant G/C;T snv 0.81; 8.0E-06 3
rs17606561
ELOVL2
1.000 0.040 6 10982126 3 prime UTR variant G/A snv 0.17 2
rs2236212
ELOVL2
1.000 0.040 6 10994782 intron variant G/C snv 0.39 2
rs9468304
ELOVL2-AS1 ; ELOVL2
1.000 0.040 6 11041932 intron variant G/A snv 0.19 2
rs174550
FADS1 ; FADS2
0.925 0.160 11 61804006 5 prime UTR variant T/C snv 0.28 13
rs174556
FADS2 ; FADS1
0.925 0.160 11 61813163 intron variant C/T snv 0.26 7
rs2911711 0.925 0.120 2 27527679 downstream gene variant T/A snv 0.58 6
rs4666002
ZNF512
0.925 0.120 2 27617773 intron variant G/A;C snv 6