Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs579459 0.752 0.320 9 133278724 upstream gene variant C/T snv 0.81 17
rs11065987 0.807 0.280 12 111634620 intergenic variant A/G snv 0.29 12
rs3764261 0.732 0.280 16 56959412 upstream gene variant C/A snv 0.31 11
rs602633 0.851 0.080 1 109278889 downstream gene variant T/G snv 0.63 8
rs9326246 0.925 0.040 11 116741017 intergenic variant C/G snv 0.93 8
rs11206510 0.763 0.240 1 55030366 intergenic variant T/A;C;G snv 7
rs11902417 2 20976028 intergenic variant G/A snv 0.25 7
rs17321515 0.776 0.200 8 125474167 intron variant A/G snv 0.49 7
rs2954029 0.807 0.160 8 125478730 intron variant A/T snv 0.42 7
rs635634 0.882 0.160 9 133279427 upstream gene variant T/A;C snv 7
rs10402271 1.000 0.080 19 44825957 downstream gene variant T/G snv 0.28 6
rs11668477 0.925 0.080 19 11084354 downstream gene variant A/G snv 0.34 6
rs2001844 0.882 0.040 8 125466503 upstream gene variant A/G snv 0.43 6
rs2001945 8 125465736 upstream gene variant G/A;C;T snv 6
rs2965101 1.000 0.080 19 44734556 intergenic variant T/C snv 0.34 6
rs2980869 8 125476008 intron variant C/T snv 0.48 6
rs2980875 8 125469505 intron variant A/C;G;T snv 6
rs2980880 8 125468730 intron variant G/A snv 0.69 6
rs515135 0.807 0.160 2 21063185 intergenic variant T/C snv 0.73 6
rs562338 0.807 0.160 2 21065449 intergenic variant A/G snv 0.69 6
rs583104 1 109278685 downstream gene variant G/T snv 0.63 6
rs6982636 8 125467073 intron variant G/A snv 0.43 6
rs9622186 22 35377961 upstream gene variant A/G snv 3.7E-03 6
rs12748152 1.000 0.120 1 26811902 upstream gene variant C/T snv 5.7E-02 5
rs1531517 1.000 0.080 19 44738916 intergenic variant G/A snv 0.11 5