Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1194611372 0.763 0.320 1 152032679 missense variant A/C snv 9
rs848 0.807 0.240 5 132660808 3 prime UTR variant A/C snv 0.67 8
rs6074028 1.000 0.040 20 46126219 intron variant A/C;G snv 1
rs2228570
VDR
0.521 0.760 12 47879112 start lost A/C;G;T snv 0.63 99
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs2476601 0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 121
rs3746444 0.514 0.760 20 34990448 mature miRNA variant A/G snv 0.20 0.19 105
rs731236
VDR
0.542 0.760 12 47844974 synonymous variant A/G snv 0.33 0.34 81
rs20541 0.585 0.720 5 132660272 missense variant A/G snv 0.72 0.77 52
rs2670660 0.708 0.400 17 5615686 intron variant A/G snv 0.41 15
rs11747270 0.790 0.240 5 150879305 intron variant A/G snv 0.21 7
rs10491322 0.925 0.120 5 134194449 3 prime UTR variant A/G snv 9.5E-02 3
rs4986790 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs2248098
VDR
0.925 0.120 12 47859573 intron variant A/G;T snv 4
rs2165667 0.925 0.040 4 186540475 intron variant A/G;T snv 2
rs7033979 0.925 0.040 9 92461698 intron variant A/G;T snv 2
rs12150220 0.724 0.360 17 5582047 missense variant A/T snv 0.37 0.33 14
rs7975232
VDR
0.576 0.760 12 47845054 intron variant C/A snv 0.51 0.55 56
rs28936375 0.752 0.320 1 53197092 missense variant C/A snv 1.7E-04 2.2E-04 15
rs1057523354 0.763 0.480 13 110179387 missense variant C/A snv 13
rs778767225
MOK
0.851 0.200 14 102231805 missense variant C/A snv 2.4E-05 7.0E-06 4
rs1544410
VDR
0.542 0.760 12 47846052 intron variant C/A;G;T snv 78
rs28940580 0.742 0.560 16 3243447 missense variant C/A;G;T snv 1.0E-04; 8.0E-06 17
rs4760648
VDR
0.851 0.200 12 47886882 intron variant C/A;G;T snv 4
rs10036748 0.752 0.360 5 151078585 intron variant C/A;T snv 11