Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
rs34933034
CSK
0.925 0.120 15 74787133 intron variant G/A;T snv 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
rs494620 0.925 0.120 6 31870936 stop gained G/A;T snv 0.44; 4.1E-06 3
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
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
rs9267531 0.882 0.120 6 31668965 non coding transcript exon variant A/G snv 7.5E-02 3
rs10954214 0.851 0.160 7 128949579 3 prime UTR variant C/T snv 0.64 4
rs11085725 0.851 0.160 19 10351837 intron variant C/T snv 0.24 4
rs112846137 0.851 0.160 3 160595133 intergenic variant G/T snv 5.3E-02 4
rs1217393 0.851 0.160 1 113891324 intron variant G/A snv 0.42 4
rs13389408 0.851 0.160 2 191068557 3 prime UTR variant T/C snv 7.4E-02 4
rs13447 0.882 0.200 7 75166663 non coding transcript exon variant T/A;C snv 1.9E-02 4