Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs372805579
CARD14
0.851 0.200 17 80195302 missense variant G/A snv 2.4E-05 2.8E-05 5
rs372878791
PRNP
1.000 0.120 20 4699783 missense variant C/G;T snv 3.2E-05; 4.0E-05 2
rs3764650
ABCA7
0.790 0.200 19 1046521 intron variant T/G snv 0.14 9
rs3849942
C9orf72 ; LOC107987057
0.776 0.200 9 27543283 non coding transcript exon variant T/A;C snv 9
rs3851179 0.752 0.280 11 86157598 downstream gene variant T/C snv 0.70 15
rs3865444
CD33
0.851 0.160 19 51224706 upstream gene variant C/A snv 0.25 8
rs393152
LINC02210 ; LINC02210-CRHR1
0.851 0.160 17 45641777 non coding transcript exon variant A/G snv 0.18 0.29 7
rs398122370
PRNP
0.925 0.160 20 4699851 missense variant G/C snv 4
rs398122414
PRNP
0.925 0.120 20 4699898 stop gained C/A snv 3
rs4538475
BST1
1.000 0.040 4 15736314 intron variant A/G snv 0.24 2
rs597668
BLOC1S3 ; MARK4
0.925 0.080 19 45205630 intron variant T/A;C;G snv 3
rs6052751
RPS4XP2
20 4664427 intron variant G/A;C snv 1
rs6107516
PRNP
1.000 0.120 20 4696446 intron variant G/A snv 0.23 2
rs610932
MS4A6A
0.851 0.080 11 60171834 downstream gene variant T/G snv 0.57 5
rs6116477 20 4704015 downstream gene variant T/C snv 0.23 1
rs670139
MS4A4A ; MS4A4E
0.925 0.080 11 60204322 intron variant G/A;T snv 3
rs74315401
PRNP
0.683 0.320 20 4699525 missense variant C/T snv 32
rs74315402
PRNP
0.882 0.200 20 4699570 missense variant C/T snv 7
rs74315403
PRNP
0.790 0.200 20 4699752 missense variant G/A snv 10
rs74315405
PRNP
0.827 0.160 20 4699813 missense variant T/C snv 6
rs74315406
PRNP
0.851 0.160 20 4699870 missense variant A/G snv 5
rs74315407
PRNP
0.732 0.240 20 4699848 missense variant G/A snv 8.0E-06 2.1E-05 15
rs74315408
PRNP
0.752 0.280 20 4699758 missense variant G/A snv 6.4E-05 4.2E-05 16
rs74315409
PRNP
0.742 0.240 20 4699915 missense variant T/G snv 6.0E-05 2.1E-05 13
rs74315410
PRNP
1.000 0.120 20 4699612 missense variant G/T snv 4.0E-06 2