Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12148769 15 23906947 intergenic variant G/A snv 8.9E-02 1
rs12476703 2 199254540 intergenic variant T/G snv 0.54 1
rs12571664 10 119949417 downstream gene variant T/C snv 0.16 1
rs12603280 17 6131434 intergenic variant G/A;C snv 1
rs12656569 5 169311587 intergenic variant A/C snv 0.79 1
rs12879819 14 77958440 intergenic variant C/A;G;T snv 1
rs13053505 22 38849613 intergenic variant G/A;C;T snv 1
rs13067731 3 137271149 intergenic variant C/T snv 0.18 1
rs13187289 5 134513486 upstream gene variant C/A;G snv 0.19 1
rs13196561 6 100312294 intergenic variant C/A snv 0.15 1
rs13199764 6 100296258 regulatory region variant T/C snv 0.17 1
rs1327942 13 59258976 upstream gene variant T/A snv 0.51 1
rs1347901 4 44516218 intergenic variant T/C snv 0.56 1
rs1364063 16 69554669 TF binding site variant T/C snv 0.35 1
rs141829833 3 51742088 intergenic variant C/T snv 1.4E-02 1
rs142058842 2 155765213 intergenic variant C/G snv 0.12 1
rs142252570 14 97296313 intergenic variant TTAA/- delins 4.0E-02 1
rs1452201 3 187631221 intergenic variant C/T snv 0.57 1
rs1456522 2 198904459 intron variant A/G;T snv 1
rs145812241 6 104670869 intergenic variant C/T snv 1.1E-02 1
rs1461503 11 122974367 downstream gene variant A/C snv 0.51 1
rs1526070 2 198918872 intron variant G/A snv 0.44 1
rs16918254 8 52856653 intergenic variant A/G snv 7.3E-02 1
rs16918636 11 29102635 intergenic variant T/C snv 0.17 1
rs16939126 8 75660218 intergenic variant T/C snv 0.16 1