Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1805087
MTR
0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 135
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs231775 0.504 0.720 2 203867991 missense variant A/G;T snv 0.42; 4.0E-06 115
rs1052133 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 147
rs1129055 0.724 0.400 3 122119472 missense variant G/A snv 0.30 0.25 15
rs1501299 0.597 0.720 3 186853334 intron variant G/C;T snv 52
rs17281995 0.763 0.360 3 122120794 3 prime UTR variant G/A;C snv 11
rs1801282 0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 131
rs1805192 0.510 0.840 3 12379739 missense variant C/G snv 121
rs2282679
GC
0.645 0.480 4 71742666 intron variant T/G snv 0.21 38
rs1801394 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 101
rs1799945 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 226
rs1800562 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 262
rs763780 0.531 0.720 6 52236941 missense variant T/C snv 6.7E-02 6.6E-02 87
rs3217992 0.683 0.480 9 22003224 3 prime UTR variant C/T snv 0.32 22
rs7903146 0.554 0.680 10 112998590 intron variant C/G;T snv 93
rs2228570
VDR
0.521 0.760 12 47879112 start lost A/C;G;T snv 0.63 99
rs1801275 0.581 0.680 16 27363079 missense variant A/G snv 0.25 0.36 58
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
rs878854066 0.439 0.800 17 7676153 missense variant GG/AC mnv 213
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