Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12072037 0.882 0.080 1 39954534 upstream gene variant C/A snv 6.1E-02 4
rs6950683 0.851 0.120 7 148884496 upstream gene variant T/C;G snv 4
rs748404 0.851 0.160 15 43267033 upstream gene variant T/C snv 0.17 4
rs7631358 0.851 0.080 3 189630622 upstream gene variant G/A snv 0.13 4
rs11020802 0.882 0.080 11 94493959 upstream gene variant C/A;G;T snv 3
rs11453459 0.882 0.080 19 52189696 upstream gene variant -/G delins 3
rs11878644 0.882 0.080 19 45373709 upstream gene variant T/C snv 0.53 3
rs1465952 0.882 0.080 11 4093309 upstream gene variant G/A;T snv 3
rs17658052 0.882 0.080 11 2001669 upstream gene variant G/A snv 1.6E-04 3
rs182623 0.882 0.080 6 52997060 upstream gene variant A/T snv 0.32 3
rs2735469 0.882 0.080 11 2001574 upstream gene variant A/G snv 3
rs2736107 0.882 0.080 5 1297739 upstream gene variant C/T snv 0.23 3
rs2741354 0.882 0.080 8 27557959 upstream gene variant C/T snv 0.58 3
rs2868370 0.882 0.080 7 76301483 upstream gene variant G/A snv 0.16 3
rs3829787 0.882 0.080 15 78563924 upstream gene variant C/T snv 0.27 3
rs4713354 0.882 0.080 6 30717643 upstream gene variant A/C snv 0.22 3
rs6965469 0.882 0.080 7 55017274 upstream gene variant C/A;T snv 3
rs7959801 0.882 0.080 12 120371787 upstream gene variant T/C snv 0.37 3
rs2228570
VDR
0.521 0.760 12 47879112 start lost A/C;G;T snv 0.63 99
rs9344 0.653 0.480 11 69648142 splice region variant G/A snv 0.45 0.39 34
rs2233679 0.763 0.360 19 9834678 splice region variant C/T snv 0.59 11
rs31490 0.776 0.280 5 1344343 splice region variant G/A;T snv 0.37; 8.0E-06 8
rs13306550 0.851 0.080 8 16168455 splice region variant T/C snv 9.8E-03 2.9E-03 4
rs2857261 0.851 0.160 4 141719484 splice region variant A/G snv 0.48 0.49 4
rs4072037 0.732 0.240 1 155192276 splice acceptor variant C/A;T snv 0.59 22