Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs478304 1.000 0.040 11 65726789 upstream gene variant G/T snv 0.54 1
rs2727365 1.000 0.040 11 13089937 intron variant G/A;T snv 1
rs1159268 1.000 0.040 1 218671564 regulatory region variant G/A snv 0.32 1
rs788790 1.000 0.040 1 202320478 downstream gene variant C/A snv 0.44 1
rs330071 1.000 0.040 8 9302385 intron variant G/A snv 0.25 1
rs38055 1.000 0.040 5 53264814 intergenic variant A/G snv 0.75 1
rs2901000 1.000 0.040 2 60274081 intergenic variant A/G snv 0.62 1
rs10911268 1.000 0.040 1 183153583 intergenic variant C/A snv 0.39 1
rs75430906 1.000 0.040 3 20676437 intron variant G/A snv 1.9E-02 1
rs4487353 1.000 0.040 4 123332634 intergenic variant G/A snv 0.53 1
rs629725 1.000 0.040 5 53335237 TF binding site variant T/C snv 0.74 1
rs6684868 1.000 0.040 1 218674648 TF binding site variant G/A snv 0.41 1
rs1092479 1.000 0.040 2 121011861 intergenic variant G/C snv 0.39 1
rs4118325 1 107035210 intergenic variant G/A;T snv 1
rs6954895 7 35546596 intergenic variant T/C snv 0.28 1
rs17154929 1.000 0.160 10 44029227 intergenic variant C/T snv 2.3E-02 1
rs12032996 1 33454985 intergenic variant G/A snv 0.12 1
rs35311980 2 228295484 intergenic variant C/T snv 4.9E-05 1
rs185291443 2 226120788 intergenic variant C/A;G snv 1
rs4288924 14 68835682 intergenic variant G/A;T snv 1
rs16943246 15 45428399 upstream gene variant G/A snv 0.29 1
rs35924503 2 228266570 intergenic variant T/C snv 1.5E-04 1
rs10157710 1 47496019 downstream gene variant C/T snv 0.78 1
rs13394343 2 85527219 intergenic variant C/A;T snv 1
rs12727104 1 171454028 intergenic variant G/A snv 8.3E-02 1