Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2736990
SNCA
0.882 0.080 4 89757390 intron variant G/A;T snv 4
rs3851179 0.752 0.280 11 86157598 downstream gene variant T/C snv 0.70 15
rs766487967
NPRL3 ; MPG
1.000 0.120 16 85517 missense variant G/A snv 8.0E-06 5.6E-05 2
rs372805579
CARD14
0.851 0.200 17 80195302 missense variant G/A snv 2.4E-05 2.8E-05 5
rs368821179
CARD14
0.925 0.160 17 80182758 missense variant T/C snv 8.0E-06 2.1E-05 3
rs10994443
ANK3
1.000 0.040 10 60635760 intron variant G/A snv 0.11 2
rs670139
MS4A4A ; MS4A4E
0.925 0.080 11 60204322 intron variant G/A;T snv 3
rs610932
MS4A6A
0.851 0.080 11 60171834 downstream gene variant T/G snv 0.57 5
rs10509125
ANK3
10 60167108 intron variant C/A snv 0.56 2
rs3865444
CD33
0.851 0.160 19 51224706 upstream gene variant C/A snv 0.25 8
rs9349407
CD2AP
1.000 0.080 6 47485642 intron variant G/C snv 0.23 2
rs6116477 20 4704015 downstream gene variant T/C snv 0.23 1
rs1473972013
CYP4X1
0.925 0.160 1 47035911 missense variant G/A snv 7.0E-06 3
rs74315409
PRNP
0.742 0.240 20 4699915 missense variant T/G snv 6.0E-05 2.1E-05 13
rs398122414
PRNP
0.925 0.120 20 4699898 stop gained C/A snv 3
rs1800014
PRNP
0.776 0.200 20 4699875 missense variant G/A snv 8.0E-03 2.2E-03 11
rs74315406
PRNP
0.851 0.160 20 4699870 missense variant A/G snv 5
rs751882709
PRNP
0.925 0.160 20 4699855 missense variant A/C snv 1.6E-05 2.8E-05 3
rs398122370
PRNP
0.925 0.160 20 4699851 missense variant G/C snv 4
rs74315407
PRNP
0.732 0.240 20 4699848 missense variant G/A snv 8.0E-06 2.1E-05 15
rs74315412
PRNP
0.851 0.120 20 4699843 missense variant G/A snv 6.0E-05 3.5E-05 5
rs776593792
PRNP
1.000 0.120 20 4699827 missense variant G/A snv 1.6E-05 2.8E-05 2
rs761807915
PRNP
0.925 0.120 20 4699824 missense variant G/A snv 4.0E-06 7.0E-06 4
rs768562045
PRNP
20 4699821 missense variant A/T snv 4.0E-06 1
rs28933385
PRNP
0.695 0.320 20 4699818 missense variant G/A snv 4.0E-06 25