Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121913530 0.583 0.640 12 25245351 missense variant C/A;G;T snv 63
rs1544410
VDR
0.542 0.760 12 47846052 intron variant C/A;G;T snv 78
rs2228570
VDR
0.521 0.760 12 47879112 start lost A/C;G;T snv 0.63 99
rs4759314 0.649 0.440 12 53968051 non coding transcript exon variant G/A snv 0.93 31
rs671 0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 116
rs1130409 0.555 0.720 14 20456995 missense variant T/A;C;G snv 4.0E-06; 4.0E-06; 0.42 72
rs11549465 0.597 0.680 14 61740839 missense variant C/T snv 8.8E-02 7.7E-02 55
rs11549467 0.653 0.400 14 61740857 missense variant G/A snv 8.9E-03 7.0E-03 30
rs121434592 0.595 0.640 14 104780214 missense variant C/T snv 4.0E-06 54
rs1051730 0.641 0.600 15 78601997 synonymous variant G/A snv 0.27 0.26 43
rs8034191 0.695 0.440 15 78513681 intron variant T/C snv 0.27 24
rs1258159645 0.630 0.600 16 69711128 missense variant G/A snv 7.0E-06 37
rs1800566 0.576 0.680 16 69711242 missense variant G/A snv 0.25 0.21 59
rs1042522 0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs1131691014 0.439 0.800 17 7676154 frameshift variant -/C ins 214
rs762846821 0.614 0.320 17 7675151 missense variant C/A;T snv 8.0E-06 57
rs878854066 0.439 0.800 17 7676153 missense variant GG/AC mnv 213
rs11615 0.572 0.640 19 45420395 synonymous variant A/G snv 0.50 0.55 62
rs13181 0.487 0.760 19 45351661 stop gained T/A;G snv 4.0E-06; 0.32 134
rs1799782 0.474 0.800 19 43553422 missense variant G/A snv 9.5E-02 7.0E-02 151
rs1799793 0.557 0.640 19 45364001 missense variant C/A;T snv 7.1E-06; 0.29 72
rs1801272 0.807 0.240 19 40848628 missense variant A/T snv 2.0E-02 1.8E-02 6
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
rs3212986 0.620 0.400 19 45409478 stop gained C/A;G;T snv 0.29; 4.3E-06; 4.3E-06 42