Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1544410
VDR
0.542 0.760 12 47846052 intron variant C/A;G;T snv 78
rs755622 0.611 0.720 22 23894205 intron variant G/C snv 0.26 44
rs3087456 0.742 0.480 16 10877045 intron variant G/A snv 0.53 14
rs749292 0.851 0.160 15 51266534 intron variant G/A snv 0.44 4
rs9525641 0.925 0.080 13 42573888 intron variant T/C snv 0.47 3
rs4355801 0.882 0.120 8 118911634 regulatory region variant A/G;T snv 5
rs1010184002 0.689 0.400 6 42978878 stop gained C/T snv 7.0E-06 60
rs61816761 0.658 0.640 1 152313385 stop gained G/A;T snv 9.4E-03; 8.0E-06 43
rs1064795104 0.790 0.440 2 72498492 stop gained A/C snv 17
rs751093906 0.882 0.200 8 42472255 stop gained G/A;C snv 4.0E-06 8
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs429358 0.590 0.600 19 44908684 missense variant T/C snv 0.14 0.16 66
rs61753219 0.672 0.400 6 42978330 missense variant G/A snv 3.6E-05 2.8E-05 64
rs121912438 0.605 0.520 21 31667299 missense variant G/A;C;T snv 1.2E-05; 8.0E-06 58
rs121918459 0.662 0.440 12 112450368 missense variant A/G snv 1.2E-05 7.0E-06 47
rs7412 0.641 0.640 19 44908822 missense variant C/T snv 6.2E-02 7.9E-02 47
rs1557043622 0.695 0.400 X 48909843 missense variant C/A snv 46
rs587782995 0.708 0.360 5 140114480 missense variant T/C snv 42
rs76763715
GBA
0.658 0.520 1 155235843 missense variant T/C;G snv 2.3E-03 35
rs151344517 0.742 0.320 18 12337505 missense variant C/T snv 31
rs66527965 0.763 0.240 17 50193038 missense variant C/A;T snv 31
rs5742905
CBS
0.701 0.360 21 43063074 missense variant A/G snv 22
rs1289324472
GBA
0.716 0.400 1 155236354 missense variant T/C snv 1.4E-05 21
rs587784177 0.790 0.280 5 177283827 missense variant G/A snv 20
rs2230912 0.752 0.280 12 121184393 missense variant A/G snv 0.13 0.12 16