Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs186696265 0.882 0.040 6 160690668 intergenic variant C/T snv 1.0E-02 6
rs41269133 1.000 0.040 6 160666831 intron variant T/C snv 8.8E-02 2
rs12664092 6 160527104 downstream gene variant A/C;G snv 1
rs1406888 6 160670561 intron variant C/T snv 0.46 1
rs142126734 6 160521894 upstream gene variant G/A snv 3.4E-02 1
rs144788267 6 160760843 intron variant G/A snv 6.5E-03 1
rs150571318 6 161281106 intergenic variant G/A snv 4.4E-03 1
rs17539620 6 154575101 upstream gene variant G/T snv 0.14 1
rs184278183 6 160756724 intron variant C/T snv 5.4E-03 1
rs187270959 6 159919224 downstream gene variant A/C snv 6.8E-03 1
rs2489940 6 160862897 intergenic variant G/T snv 6.5E-03 1
rs3757037 6 161276368 upstream gene variant A/G;T snv 0.44 1
rs56393506 6 160668275 intron variant C/T snv 0.17 1
rs766345636 13 51297734 TF binding site variant A/C snv 3.1E-04 1
rs9322428 6 153596811 intergenic variant T/A snv 0.46 1
rs9347800 6 157950052 downstream gene variant T/C snv 0.12 1
rs9384478 6 156595632 intergenic variant G/A snv 6.9E-02 1
rs9406316 6 157228616 intergenic variant T/C snv 0.20 1
rs754054303
ACAT2
6 159774018 intron variant A/G snv 7.3E-04 1
rs2293289
AGPAT4
6 161130407 3 prime UTR variant G/A snv 8.7E-02 1
rs9295143
AGPAT4
6 161233083 intron variant G/C;T snv 1
rs7412
APOE
0.641 0.640 19 44908822 missense variant C/T snv 6.2E-02 7.9E-02 20
rs9457516
C6orf99
6 158914219 intron variant C/T snv 0.17 1
rs767873499
DLEU1
13 50339520 intron variant G/C snv 2.9E-04 1
rs749307626
DLEU2
13 50055529 intron variant T/C snv 2.9E-04 1