Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs204999 0.763 0.480 6 32142202 intergenic variant A/G snv 0.28 13
rs4409785 0.752 0.240 11 95578258 intron variant T/C snv 0.13 12
rs4728142 0.732 0.320 7 128933913 upstream gene variant G/A snv 0.38 12
rs6457617 0.763 0.480 6 32696074 intergenic variant C/A;T snv 9
rs9271366 0.807 0.240 6 32619077 intergenic variant G/A snv 0.86 9
rs9275572 0.724 0.360 6 32711222 upstream gene variant A/G;T snv 9
rs2327832 0.790 0.320 6 137651931 intergenic variant A/G snv 0.16 7
rs2736340 0.683 0.480 8 11486464 upstream gene variant C/T snv 0.25 7
rs2844511 0.807 0.200 6 31422007 intron variant A/G;T snv 7
rs2872507 0.752 0.360 17 39884510 intergenic variant G/A;T snv 7
rs6920220 0.742 0.440 6 137685367 intron variant G/A snv 0.16 7
rs9275524 0.807 0.160 6 32707332 upstream gene variant T/C snv 0.58 7
rs1329568 0.882 0.120 9 37037979 upstream gene variant T/A;G snv 6
rs1569723 0.851 0.280 20 46113425 upstream gene variant C/A snv 0.80 6
rs1794282 0.807 0.320 6 32698749 intergenic variant C/T snv 6.4E-02 6
rs2542151 0.763 0.480 18 12779948 upstream gene variant G/T snv 0.83 6
rs2647012 0.790 0.320 6 32696681 intergenic variant T/C snv 0.64 6
rs2844513 0.925 0.120 6 31420437 intron variant G/A snv 0.53 6
rs3129763 0.827 0.280 6 32623148 TF binding site variant G/A snv 0.23 6
rs7762279 0.807 0.360 6 32787513 intergenic variant T/C snv 8.4E-02 6
rs7774434 0.807 0.360 6 32689801 TF binding site variant T/C snv 0.40 6
rs9275141 0.827 0.240 6 32683340 intergenic variant T/G snv 0.50 6
rs9275312 0.807 0.280 6 32697951 intergenic variant A/G snv 0.16 6
rs2395174 0.827 0.320 6 32437101 upstream gene variant T/G snv 0.24 5
rs2428486 0.925 0.120 6 31386327 upstream gene variant T/C snv 0.42 5