Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs113488022 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490
rs121913377 0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
rs2228570
VDR
0.521 0.760 12 47879112 start lost A/C;G;T snv 0.63 99
rs1544410
VDR
0.542 0.760 12 47846052 intron variant C/A;G;T snv 78
rs11554290 0.583 0.600 1 114713908 missense variant T/A;C;G snv 59
rs397517132 0.623 0.280 7 55191846 missense variant A/T snv 48
rs121913355 0.641 0.520 7 140781602 missense variant C/A;G;T snv 4.0E-06 42
rs1057519695 0.641 0.520 1 114713907 missense variant TT/CA;CC mnv 35
rs121913364 0.641 0.520 7 140753334 missense variant T/C;G snv 4.0E-06 34
rs121913227 0.653 0.320 7 140753336 missense variant AC/CT;TT mnv 31
rs1057519834 0.658 0.480 1 114713908 missense variant TG/CT mnv 31
rs121913254 0.658 0.440 1 114713909 stop gained G/A;C;T snv 31
rs121913255 0.667 0.400 1 114713907 missense variant T/A;G snv 26
rs121913366 0.763 0.400 7 140753345 missense variant A/C;T snv 12
rs121913378 0.776 0.280 7 140753337 missense variant C/A;G;T snv 11
rs104894095 0.827 0.120 9 21971200 missense variant C/G;T snv 9.0E-06 6
rs993022333
KIT
0.851 0.080 4 54733173 missense variant A/C;T snv 5
rs1024708183 0.925 0.040 19 7909761 missense variant A/G snv 4
rs750697353 0.882 0.080 3 12608919 missense variant C/T snv 1.2E-05 2.8E-05 4
rs121913368 0.925 0.040 7 140753345 missense variant AG/GA mnv 2
rs868224085 1.000 0.040 2 221482474 missense variant G/A snv 1
rs267601191 1.000 0.040 7 100819817 missense variant G/A snv 1
rs1451501407 1.000 0.040 17 8006628 missense variant G/A snv 1
rs1238066548 1.000 0.040 19 38595699 missense variant G/A;T snv 1
rs267601046 1.000 0.040 6 43283303 missense variant C/T snv 1