Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3819025 0.752 0.480 6 52186476 intron variant G/A snv 0.13 8.5E-02 11
rs8193037 0.752 0.320 6 52186311 upstream gene variant G/A;T snv 12
rs2275913 0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28 105
rs3819024 0.701 0.560 6 52185988 upstream gene variant A/G snv 0.34 17
rs8193036 0.689 0.600 6 52185695 upstream gene variant C/T snv 0.72 21
rs4711998 0.708 0.360 6 52185555 upstream gene variant A/G snv 0.64 16
rs2043211 0.653 0.480 19 48234449 missense variant A/T snv 0.33 0.29 29
rs2228570
VDR
0.521 0.760 12 47879112 start lost A/C;G;T snv 0.63 99
rs1883832 0.581 0.680 20 46118343 5 prime UTR variant T/C snv 0.75 0.80 52
rs775144154 0.627 0.600 21 45531904 missense variant C/A;T snv 9.7E-06; 1.4E-05 38
rs4420638 0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 43
rs501120 0.763 0.240 10 44258419 downstream gene variant T/C snv 0.24 10
rs3025039 0.576 0.720 6 43784799 3 prime UTR variant C/T snv 0.13 62
rs1222213359 0.574 0.720 6 43770966 missense variant G/A snv 62
rs2010963 0.542 0.840 6 43770613 5 prime UTR variant C/G snv 0.68 82
rs1570360 0.641 0.680 6 43770093 upstream gene variant A/G snv 0.76 38
rs699947 0.570 0.680 6 43768652 upstream gene variant A/C;T snv 67
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
rs7984870 0.925 0.160 13 42572346 intron variant G/C snv 0.46 2
rs1800469 0.547 0.760 19 41354391 intron variant A/G snv 0.69 78
rs1800470 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 107
rs3746444 0.514 0.760 20 34990448 mature miRNA variant A/G snv 0.20 0.19 105
rs1024611 0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28 63
rs1800625 0.641 0.680 6 32184665 upstream gene variant A/G snv 0.15 39