Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs174536
TMEM258 ; MYRF
11 61784455 non coding transcript exon variant A/C snv 0.29 2
rs174574
FADS2
1.000 0.080 11 61832870 intron variant A/C snv 0.55 2
rs1077989
GPHN ; TMEM229B
1.000 0.080 14 67509105 intron variant A/C snv 0.39 1
rs17764682
ELOVL2-AS1
6 11058582 intron variant A/C snv 0.24 1
rs2391388
ALG14
1 95020269 intron variant A/C snv 0.49 1
rs3798721
ELOVL2
6 11039950 intron variant A/C snv 0.31 1
rs6671200
TLCD4-RWDD3 ; LOC101928118
1 95231973 intron variant A/C snv 0.90 1
rs17148090
DLG2
11 85306432 intron variant A/C;G snv 7.4E-02 1
rs17764592
ELOVL2
6 11002911 intron variant A/C;G snv 1
rs7394871
FADS3
11 61885042 intron variant A/C;T snv 2
rs10792320 11 61978819 intergenic variant A/C;T snv 1
rs1535
FADS2
0.752 0.240 11 61830500 intron variant A/G snv 0.31 10
rs1260333 0.882 0.160 2 27525757 downstream gene variant A/G snv 0.58 8
rs2851682
FADS2
11 61848540 intron variant A/G snv 9.9E-02 5
rs7200543
PDXDC1
16 15036113 synonymous variant A/G snv 0.35 0.30 4
rs174534
MYRF ; TMEM258
1.000 0.080 11 61781986 non coding transcript exon variant A/G snv 0.28 3
rs1000778
FADS3
1.000 0.040 11 61887833 intron variant A/G snv 0.59 2
rs174464
FADS3
11 61890454 intron variant A/G snv 0.59 2
rs174472
RAB3IL1
11 61904484 intron variant A/G snv 0.41 2
rs2072114
FADS2
1.000 0.080 11 61837743 intron variant A/G snv 0.19 0.16 2
rs2727266
RAB3IL1
11 61936862 upstream gene variant A/G snv 9.8E-02 2
rs2845573
FADS2
1.000 0.040 11 61834436 intron variant A/G snv 9.7E-02 2
rs509360
MYRF ; TMEM258
11 61781087 intron variant A/G snv 0.61 0.52 2
rs10885997
PNLIPRP2
10 116638460 synonymous variant A/G snv 0.38 0.36 1
rs11190604
HIF1AN
10 100542700 intron variant A/G snv 0.19 1