Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
rs1531517 1.000 0.080 19 44738916 intergenic variant G/A snv 0.11 5
rs16996148 0.882 0.120 19 19547663 downstream gene variant G/T snv 0.10 5
rs2927438 0.925 0.080 19 44738850 intergenic variant G/A snv 0.20 5
rs2954021 1.000 0.040 8 125469835 intron variant A/G snv 0.54 5
rs4938303 11 116714271 intergenic variant C/A;T snv 0.62 5
rs10156121 7 142672656 downstream gene variant T/C snv 3.9E-02 4
rs10808546 8 125483576 intron variant C/T snv 0.39 4
rs247617 0.827 0.160 16 56956804 regulatory region variant C/A snv 0.29 4
rs2523575 6 31361049 upstream gene variant C/G snv 0.20 4
rs2954031 8 125479491 intron variant G/T snv 0.42 4
rs2954033 8 125481504 intron variant A/G snv 0.76 4
rs439401 0.851 0.200 19 44911194 non coding transcript exon variant T/C snv 0.68 4
rs4871603 8 125468125 intron variant C/T snv 0.59 4
rs585362 1 109247173 upstream gene variant C/G;T snv 4
rs6734238 1.000 0.080 2 113083453 upstream gene variant A/G snv 0.39 4
rs754523 2 21088819 intergenic variant A/G snv 0.28 4
rs754524 2 21088669 intergenic variant T/G snv 0.19 4