Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2857595 0.827 0.320 6 31600692 intergenic variant G/A snv 0.27 6
rs12477314 2 238955452 regulatory region variant C/G;T snv 3
rs13118928 0.925 0.040 4 144565237 intron variant A/G snv 0.33 3
rs13141641 1.000 0.040 4 144585304 intron variant T/C snv 0.32 3
rs1980057 1.000 0.040 4 144564586 intron variant C/T snv 0.31 3
rs2036527 0.851 0.080 15 78559273 regulatory region variant G/A snv 0.29 3
rs7763064 6 142476152 intergenic variant G/A snv 0.38 3
rs10824425 10 76580552 intergenic variant G/C snv 0.42 2
rs12664563 6 142464064 intergenic variant A/G snv 0.21 2
rs1512288 1.000 0.040 4 144570129 intron variant G/A snv 0.42 2
rs1541374 4 105127203 intergenic variant T/A;G snv 2
rs155259 6 142525428 downstream gene variant G/A snv 0.39 2
rs16909856 9 95442211 downstream gene variant G/A;C;T snv 2
rs1928528 6 142457972 intergenic variant T/G snv 0.21 2
rs2114719 15 70640999 downstream gene variant A/G;T snv 2
rs2162555 15 70641233 downstream gene variant T/C snv 0.85 2
rs262114 6 142497081 intergenic variant C/T snv 0.39 2
rs262115 6 142496270 intergenic variant T/C snv 0.51 2
rs262119 6 142521656 downstream gene variant T/C snv 0.45 2
rs262120 6 142521223 intergenic variant C/A snv 0.20 2
rs262121 6 142518361 regulatory region variant T/C;G snv 2
rs2637261 10 76560835 non coding transcript exon variant C/T snv 0.54 2
rs2637266 10 76571560 intergenic variant A/G snv 0.48 2
rs4747972 10 12263649 TF binding site variant G/C snv 0.45 2
rs643975 6 142523114 downstream gene variant C/G snv 0.20 2