Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1416580204
MOK
0.608 0.720 14 102250837 missense variant C/T snv 4.0E-06 7.0E-06 49
rs5498 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 99
rs861539 0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 104
rs1143623 0.677 0.440 2 112838252 upstream gene variant C/G snv 0.24 29
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1801133 0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 174
rs895819 0.623 0.560 19 13836478 non coding transcript exon variant T/A;C;G snv 0.34 0.38 46
rs4880 0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 131
rs4402960 0.724 0.400 3 185793899 intron variant G/T snv 0.38 21
rs2241766 0.608 0.720 3 186853103 synonymous variant T/C;G snv 8.0E-06; 0.13 48
rs4680 0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs1805087
MTR
0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 135
rs2070600 0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 82
rs1800470 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 107
rs1982073 0.649 0.640 19 41353016 missense variant G/A;C snv 32
rs25487 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs1799782 0.474 0.800 19 43553422 missense variant G/A snv 9.5E-02 7.0E-02 151
rs731236
VDR
0.542 0.760 12 47844974 synonymous variant A/G snv 0.33 0.34 81
rs1544410
VDR
0.542 0.760 12 47846052 intron variant C/A;G;T snv 78
rs758272654 0.611 0.680 20 58909201 synonymous variant T/C snv 4.0E-06 7.0E-06 50
rs1137100 0.627 0.640 1 65570758 missense variant A/G snv 0.30 0.25 39
rs1137101 0.554 0.760 1 65592830 missense variant A/G snv 0.51 0.50 77
rs1805094 0.716 0.440 1 65610269 missense variant G/C;T snv 0.16; 4.0E-06 16
rs1695 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188