Disease: Body mass index procedure
Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs13386964 2 650828 regulatory region variant G/A snv 0.18 2
rs13388043 2 637597 regulatory region variant C/A;T snv 2
rs13393304 2 637830 regulatory region variant A/C;G snv 2
rs13396935 2 653195 intergenic variant G/A snv 0.18 2
rs13397165 2 653354 intergenic variant G/A snv 0.18 2
rs13401686 2 650519 regulatory region variant A/G snv 0.18 2
rs13415094 2 653093 intergenic variant T/C snv 0.19 2
rs1555543 1 96479241 intergenic variant A/C snv 0.55 2
rs16858082 4 45173787 intergenic variant T/C snv 0.41 2
rs17700144 1.000 0.080 18 60144750 intron variant G/A snv 0.14 4
rs17782313 0.683 0.480 18 60183864 intergenic variant T/C snv 0.24 6
rs2331841 1.000 0.080 18 60161404 upstream gene variant G/A snv 0.43 2
rs2867108 2 650143 intergenic variant T/C snv 0.18 2
rs2867109 2 651030 regulatory region variant T/G snv 0.18 2
rs2867110 2 651105 regulatory region variant G/C snv 0.18 2
rs2867112 2 651349 intergenic variant T/G snv 0.18 2
rs2867113 2 651365 intergenic variant G/A snv 0.18 2
rs2867125 0.925 0.120 2 622827 intergenic variant T/A;C snv 0.85 3
rs2890652 2 142202362 intergenic variant T/C snv 0.21 2
rs2903492 2 624678 intergenic variant G/A snv 0.85 2
rs2922763 8 75661476 intergenic variant G/T snv 0.77 2
rs29941 1.000 0.080 19 33818627 downstream gene variant A/G snv 0.70 3
rs34572584 4 170869381 intergenic variant G/T snv 3.3E-02 2
rs348495 4 45182425 intergenic variant G/A snv 0.49 2
rs4423631 2 648758 intergenic variant T/A;C;G snv 2