Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2954021 1.000 0.040 8 125469835 intron variant A/G snv 0.54 13
rs1128249
COBLL1
1.000 0.080 2 164672114 intron variant G/C;T snv 9
rs174577
FADS2
1.000 0.080 11 61837342 intron variant C/A snv 0.38 9
rs2925979
CMIP
1.000 0.080 16 81501185 intron variant T/A;C snv 9
rs9987289
LOC157273
1.000 0.040 8 9325848 non coding transcript exon variant A/G snv 0.87 8
rs7607980
COBLL1
1.000 0.080 2 164694691 missense variant T/C snv 0.11 0.13 7
rs11048456
LOC105369705
1.000 0.080 12 26310149 intron variant C/T snv 0.62 6
rs12423664
FBRSL1
1.000 0.040 12 132493308 intron variant G/A snv 0.10 6
rs12748152 1.000 0.120 1 26811902 upstream gene variant C/T snv 5.7E-02 6
rs174554
FADS1 ; FADS2
1.000 0.080 11 61811991 intron variant A/G snv 0.40 0.28 6
rs1800978
ABCA1
1.000 0.040 9 104903697 5 prime UTR variant C/A;G;T snv 5.4E-06; 0.14 6
rs247616 1.000 0.040 16 56955678 intergenic variant C/T snv 0.29 6
rs10184004 1.000 0.080 2 164651879 downstream gene variant C/T snv 0.48 5
rs1045241
TNFAIP8
1.000 0.120 5 119393591 3 prime UTR variant C/T snv 0.30 5
rs12686004
ABCA1
1.000 0.040 9 104891145 intron variant G/A snv 9.1E-02 5
rs13389219
COBLL1
1.000 0.080 2 164672366 intron variant C/T snv 0.47 5
rs15285
LPL
1.000 0.040 8 19967156 3 prime UTR variant C/T snv 0.36 5
rs2278426
ANGPTL8 ; DOCK6
1.000 0.080 19 11239812 missense variant C/T snv 0.11 0.11 5
rs2294915
PNPLA3
1.000 0.040 22 43945024 intron variant C/G;T snv 5
rs2678379
APOB
1.000 0.080 2 21003688 intron variant A/G snv 0.76 5
rs3768321
PABPC4 ; PABPC4-AS1
1.000 0.080 1 39570256 intron variant G/T snv 0.14 5
rs895953
SETD1B
1.000 0.040 12 121811142 intron variant G/T snv 0.76 5
rs10402271 1.000 0.080 19 44825957 downstream gene variant T/G snv 0.28 4
rs12801636
PCNX3
1.000 0.040 11 65623846 intron variant G/A snv 0.25 4
rs1531517 1.000 0.080 19 44738916 intergenic variant G/A snv 0.11 4