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
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs6265 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs4680 0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs759834365 0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237
rs1045642 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs1801133 0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 174
rs662 0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 157
rs1805087
MTR
0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 135
rs2228570
VDR
0.521 0.760 12 47879112 start lost A/C;G;T snv 0.63 99
rs2032582 0.538 0.800 7 87531302 missense variant A/C;T snv 0.54; 3.8E-02 97
rs16944 0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 92
rs2010963 0.542 0.840 6 43770613 5 prime UTR variant C/G snv 0.68 82
rs6313 0.562 0.640 13 46895805 synonymous variant G/A snv 0.41 0.40 82
rs2234693 0.555 0.680 6 151842200 intron variant T/C snv 0.47 77
rs25531 0.581 0.520 17 30237328 upstream gene variant T/C snv 0.18 72
rs1128503 0.564 0.760 7 87550285 synonymous variant A/G snv 0.54 0.63 64
rs9340799 0.583 0.680 6 151842246 intron variant A/G snv 0.32 62
rs1800497 0.620 0.400 11 113400106 missense variant G/A snv 0.26 0.26 56
rs953038635 0.590 0.800 6 159692720 missense variant G/A;T snv 8.0E-06 51
rs6277 0.689 0.480 11 113412737 synonymous variant G/A snv 0.41 0.38 36
rs746682028 0.645 0.480 11 27658414 missense variant C/A;T snv 4.0E-06; 4.0E-06 36
rs4986938 0.641 0.600 14 64233098 3 prime UTR variant C/T snv 0.31 0.33 35
rs1256049 0.645 0.560 14 64257333 synonymous variant C/T snv 6.7E-02 6.3E-02 32
rs4818 0.683 0.440 22 19963684 synonymous variant C/G;T snv 0.34 27