Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1799782 0.474 0.800 19 43553422 missense variant G/A snv 9.5E-02 7.0E-02 151
rs25487 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs25489 0.550 0.720 19 43552260 missense variant C/G;T snv 8.5E-06; 7.1E-02 78
rs774359492 0.807 0.200 14 55008684 missense variant C/T snv 4.0E-06 7.0E-06 7
rs7097397 0.925 0.120 10 48817351 missense variant G/A snv 0.38 0.31 2
rs707928 0.827 0.320 6 31774813 intron variant A/G snv 0.47 5
rs1222213359 0.574 0.720 6 43770966 missense variant G/A snv 62
rs2010963 0.542 0.840 6 43770613 5 prime UTR variant C/G snv 0.68 82
rs2228570
VDR
0.521 0.760 12 47879112 start lost A/C;G;T snv 0.63 99
rs3890733
VDR
0.882 0.120 12 47895590 intron variant C/T snv 0.27 3
rs4760648
VDR
0.851 0.200 12 47886882 intron variant C/A;G;T snv 4
rs7975232
VDR
0.576 0.760 12 47845054 intron variant C/A snv 0.51 0.55 56
rs2283790 0.882 0.120 22 21602364 intron variant A/G snv 0.21 3
rs11203203 0.807 0.240 21 42416077 intron variant G/A snv 0.28 9
rs1893592 0.742 0.280 21 42434957 missense variant A/C;G snv 0.27; 8.0E-06 12
rs2277798 0.925 0.120 21 42403997 missense variant A/G snv 0.55 0.60 3
rs1448674651 0.667 0.560 18 671384 missense variant G/A;C snv 4.0E-06 23
rs11085725 0.851 0.160 19 10351837 intron variant C/T snv 0.24 4
rs34536443 0.667 0.400 19 10352442 missense variant G/C snv 2.7E-02 2.8E-02 25
rs35018800 0.790 0.160 19 10354167 missense variant G/A snv 4.6E-03 4.9E-03 9
rs6457536 0.882 0.200 6 32305988 intron variant A/G snv 0.21 3
rs6935269 0.925 0.120 6 32292573 intron variant T/C snv 0.25 2
rs1003878 0.882 0.200 6 32332045 stop gained G/A snv 0.19 0.23 3
rs3129939 0.827 0.360 6 32368989 intron variant A/G snv 0.14 5
rs3129943 0.851 0.240 6 32370918 intron variant A/G snv 0.26 4