Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs13447 0.882 0.200 7 75166663 non coding transcript exon variant T/A;C snv 1.9E-02 4
rs17581834 0.882 0.120 1 206802774 intron variant T/C snv 4.2E-02 3
rs201802880 0.882 0.200 7 74779296 missense variant G/A snv 1.1E-03 4
rs2242665 0.882 0.160 6 31871532 missense variant C/T snv 0.60 0.60 3
rs2248932
BLK
0.882 0.160 8 11534141 intron variant A/G snv 0.60 3
rs2283790 0.882 0.120 22 21602364 intron variant A/G snv 0.21 3
rs2377422 0.882 0.200 12 8128312 intron variant C/T snv 0.60 3
rs2596501 0.882 0.200 6 31353434 intron variant C/T snv 0.57 3
rs2844635 0.882 0.200 6 31107704 downstream gene variant A/G snv 0.37 3
rs3844283 0.882 0.200 3 10222796 missense variant C/G snv 0.37 0.35 3
rs3890733
VDR
0.882 0.120 12 47895590 intron variant C/T snv 0.27 3
rs437179 0.882 0.160 6 31961237 missense variant A/C snv 0.76 0.78 3
rs4937333 0.882 0.120 11 128460625 3 prime UTR variant T/C snv 0.45 4
rs5029937 0.882 0.160 6 137874014 intron variant G/T snv 0.13 4
rs535586 0.882 0.160 6 31892560 splice region variant T/A;C snv 0.77 3
rs644827 0.882 0.160 6 31870664 missense variant T/C snv 0.60 0.60 3
rs6457536 0.882 0.200 6 32305988 intron variant A/G snv 0.21 3
rs659445 0.882 0.160 6 31896527 intron variant G/A;C snv 0.77 0.76 3
rs660550 0.882 0.160 6 31869500 intron variant C/A;G snv 0.60 3
rs7579944 0.882 0.200 2 30222160 intergenic variant T/C;G snv 5
rs7745656 0.882 0.200 6 32713193 upstream gene variant G/T snv 0.29 3
rs7758736 0.882 0.200 6 32790617 intergenic variant G/A snv 0.14 3
rs799454 0.882 0.200 14 34927973 intron variant A/G snv 0.45 3
rs878081 0.882 0.200 21 44288394 synonymous variant C/T snv 0.21 0.19 3
rs922483
BLK
0.882 0.200 8 11494403 5 prime UTR variant C/T snv 0.31 3