Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs231775 0.504 0.720 2 203867991 missense variant A/G;T snv 0.42; 4.0E-06 115
rs281864719
ALK
0.763 0.240 2 29220831 missense variant A/C;G;T snv 14
rs281864720
ALK
0.925 0.040 2 29213994 missense variant A/C;G;T snv 4
rs28934906 0.716 0.320 X 154031355 missense variant G/A snv 46
rs368311455 0.882 0.200 1 53211185 missense variant C/T snv 3.2E-05 2.8E-05 4
rs3829251 0.851 0.120 11 71483513 intron variant G/A snv 0.21 8
rs397514611 1.000 6 5545261 missense variant T/C snv 1.2E-05 2
rs397514612 1.000 6 5613275 missense variant A/T snv 1.6E-05 7.0E-06 2
rs4516035
VDR
0.776 0.360 12 47906043 non coding transcript exon variant T/C snv 0.31 10
rs483352809 0.882 0.120 19 6495754 missense variant C/T snv 5
rs4945008 1.000 0.080 11 71510202 intron variant A/G;T snv 2
rs527236031 0.882 0.080 20 45424323 missense variant C/T snv 1.6E-05 4.2E-05 5
rs587776983 0.807 0.240 19 6502209 missense variant G/A;C;T snv 9
rs587777606 0.851 0.160 11 62691300 stop gained G/A snv 4.0E-06 7.0E-06 6
rs7041
GC
0.576 0.800 4 71752617 missense variant A/C;T snv 0.52; 4.0E-06 64
rs7116978 1.000 0.080 11 14860225 intron variant T/C snv 0.65 2
rs74315403 0.790 0.200 20 4699752 missense variant G/A snv 10
rs74315413 0.807 0.160 20 4699780 missense variant A/G snv 8
rs745386663 0.807 0.160 3 33051956 missense variant G/A snv 8.0E-06 2.1E-05 7
rs751557097 1 53213431 missense variant G/C snv 2.8E-05 1
rs751866383 1.000 0.040 4 39470047 missense variant G/T snv 4.0E-06 3
rs752874517 1.000 0.080 20 45425779 missense variant C/A;T snv 8.0E-06 7.0E-06 2
rs755090271 X 19359501 missense variant G/A;C snv 5.4E-06; 5.4E-06 1
rs756632799 0.882 0.080 20 45416579 stop gained G/T snv 1.6E-05 7.0E-06 5
rs756712426 15 78166196 missense variant C/A snv 2.0E-05 1