Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9277557 1.000 0.080 6 33088917 3 prime UTR variant T/C snv 0.25 1
rs9277554 0.790 0.520 6 33087761 3 prime UTR variant C/T snv 0.38 7
rs9277551 1.000 0.080 6 33087717 3 prime UTR variant G/A;T snv 1
rs9277550 0.925 0.200 6 33087710 3 prime UTR variant T/C snv 0.38 2
rs9277549 1.000 0.080 6 33087642 3 prime UTR variant A/G snv 0.38 1
rs9277547 0.925 0.200 6 33087590 3 prime UTR variant C/A snv 0.38 2
rs9277546 0.925 0.200 6 33087569 3 prime UTR variant T/G snv 0.38 2
rs9277542 0.851 0.280 6 33087470 3 prime UTR variant T/A;C snv 4
rs9277541 0.925 0.200 6 33087381 3 prime UTR variant A/G;T snv 2
rs9277540 0.925 0.200 6 33087346 3 prime UTR variant A/G snv 0.38 2
rs9277538 0.925 0.200 6 33087270 3 prime UTR variant A/G snv 0.38 2
rs9277535 0.724 0.440 6 33087084 3 prime UTR variant A/G snv 0.25 13
rs9277534 0.790 0.280 6 33087030 3 prime UTR variant A/G snv 0.38 7
rs9277533 0.925 0.200 6 33086944 3 prime UTR variant C/T snv 0.38 2
rs9277515 0.925 0.200 6 33086491 intron variant C/A;T snv 8.3E-03; 7.4E-06 2
rs9277495 1.000 0.080 6 33086294 intron variant G/C snv 0.38 1
rs9277492 0.925 0.200 6 33086205 intron variant G/A;C snv 4.4E-06; 0.28 2
rs9277488 1.000 0.080 6 33086129 intron variant G/T snv 0.38 1
rs9277480 1.000 0.080 6 33086035 intron variant A/G snv 0.25 1
rs9277479 0.925 0.200 6 33086012 intron variant A/G snv 0.38 2
rs9277477 0.925 0.200 6 33085995 intron variant G/A;T snv 2
rs9277472 1.000 0.080 6 33085946 intron variant T/C snv 0.31 0.38 1
rs9277471 1.000 0.080 6 33085905 missense variant G/A;C snv 0.32; 4.1E-06 1
rs9277469 0.925 0.200 6 33085691 intron variant G/T snv 0.38 2
rs9277468 0.925 0.200 6 33085678 intron variant C/T snv 0.38 2