Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs248831 16 11187361 intergenic variant G/A snv 0.31 1
rs8061043 16 11067072 intron variant G/T snv 0.19 1
rs62026377 16 11135271 intron variant G/T snv 0.23 1
rs6498142 16 10987392 intron variant C/G snv 0.77 1
rs876476 16 11056391 intron variant G/A snv 0.26 1
rs3862469 1.000 0.040 16 11100223 intron variant C/T snv 0.35 1
rs36045143 1.000 0.080 16 11131109 intron variant A/G snv 0.18 3
rs11645657 1.000 0.080 16 11129597 intron variant C/A;G snv 0.48 2
rs12935657 0.925 0.080 16 11125184 intron variant G/A snv 0.18 2
rs7203459 1.000 0.080 16 11136846 intron variant T/C snv 0.23 2
rs34069391 0.925 0.080 16 11067358 intron variant T/- delins 2
rs12935413 1.000 0.080 16 11116590 intron variant G/A snv 0.34 2
rs35032408 0.925 0.080 16 11121567 intron variant T/C;G snv 2
rs17806299 1.000 0.080 16 11106123 intron variant G/A snv 0.15 1
rs9923856 1.000 0.080 16 11116558 intron variant T/C snv 0.41 1
rs12708715 1.000 0.080 16 11083967 intron variant C/T snv 0.39 1
rs9652601 1.000 0.080 16 11080508 intron variant G/A snv 0.34 1
rs8054198 1.000 0.080 16 10944503 upstream gene variant C/T snv 6.7E-02 1
rs11865121 1.000 0.080 16 11072831 intron variant C/A snv 0.40 1
rs6498160 1.000 0.080 16 11105590 intron variant T/C snv 0.51 1
rs6498168 1.000 0.080 16 11141273 intron variant T/G snv 0.71 1
rs8061882 0.827 0.120 16 11067551 intron variant G/C snv 0.11 5
rs35441874 0.882 0.120 16 11119164 intron variant T/A snv 0.19 3
rs62026376 0.925 0.120 16 11134855 intron variant C/T snv 0.18 2
rs34972832 0.925 0.120 16 11105081 intron variant G/A;T snv 0.14 2