Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs117865832 16 66979753 downstream gene variant G/A snv 3.3E-02 1
rs118038583 6 135264840 downstream gene variant T/G snv 2.1E-02 1
rs12126043 1 147818675 intergenic variant G/A snv 0.14 1
rs12142550 1 154286073 upstream gene variant C/T snv 0.21 1
rs12191243 1.000 0.040 6 135125688 intergenic variant C/G snv 0.20 1
rs12413565 10 99525359 upstream gene variant C/A;T snv 1
rs12636518 3 30156262 regulatory region variant T/C snv 0.34 1
rs12652072 5 154654619 intergenic variant G/C snv 0.18 1
rs12664139 6 163335056 downstream gene variant A/T snv 0.29 1
rs1268161 6 108690630 regulatory region variant G/A snv 0.23 1
rs12706122 7 116927678 regulatory region variant G/A snv 0.27 1
rs12713575 2 66854375 regulatory region variant G/A snv 0.22 1
rs1275957 2 26674633 upstream gene variant G/C;T snv 1
rs12762783 10 3769890 downstream gene variant A/C snv 0.35 1
rs12771902 10 70242743 downstream gene variant G/A snv 0.25 1
rs12803281 11 111349569 downstream gene variant C/T snv 0.39 1
rs12885878 14 103541218 downstream gene variant A/G snv 0.71 1
rs1288650 9 88814580 TF binding site variant C/G snv 0.49 1
rs12901297 15 77094333 regulatory region variant G/A snv 0.63 1
rs12903896 15 74760154 downstream gene variant C/T snv 0.43 1
rs13141124 4 83026404 intergenic variant G/A snv 0.18 1
rs13165004 5 87019120 intron variant C/T snv 0.33 1
rs13169378 5 34514869 intergenic variant T/C snv 0.13 1
rs1320959 6 135116248 regulatory region variant T/C snv 0.37 1
rs1338219 1 219624333 intergenic variant A/C;G;T snv 1