Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2075650
TOMM40
0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 45
rs11136000
CLU
0.752 0.160 8 27607002 intron variant T/C snv 0.56 19
rs3764650
ABCA7
0.790 0.200 19 1046521 intron variant T/G snv 0.14 9
rs11767557
EPHA1-AS1
0.882 0.080 7 143412046 intron variant T/C snv 0.18 4
rs2736990
SNCA
0.882 0.080 4 89757390 intron variant G/A;T snv 4
rs12817488
CCDC62
1.000 0.040 12 122811747 intron variant G/A snv 0.39 3
rs597668
BLOC1S3 ; MARK4
0.925 0.080 19 45205630 intron variant T/A;C;G snv 3
rs670139
MS4A4A ; MS4A4E
0.925 0.080 11 60204322 intron variant G/A;T snv 3
rs10509125
ANK3
10 60167108 intron variant C/A snv 0.56 2
rs10994443
ANK3
1.000 0.040 10 60635760 intron variant G/A snv 0.11 2
rs12734001
PPP1R12B
1.000 0.080 1 202421786 intron variant C/T snv 3.5E-05 2
rs1994090
SLC2A13
1.000 0.040 12 40034759 intron variant G/A;T snv 2
rs4538475
BST1
1.000 0.040 4 15736314 intron variant A/G snv 0.24 2
rs6107516
PRNP
1.000 0.120 20 4696446 intron variant G/A snv 0.23 2
rs9349407
CD2AP
1.000 0.080 6 47485642 intron variant G/C snv 0.23 2
rs1016726
CHN2
7 29316787 intron variant G/A snv 0.12 1
rs2756271
RPS4XP2 ; PRNP
20 4684616 intron variant A/G;T snv 1
rs6052751
RPS4XP2
20 4664427 intron variant G/A;C snv 1
rs767181086
LAMC2
0.827 0.240 1 183220922 stop gained G/A;T snv 8.0E-06; 4.0E-06 11
rs80356711
PRNP
1.000 20 4699698 stop gained C/T snv 4
rs398122414
PRNP
0.925 0.120 20 4699898 stop gained C/A snv 3
rs80356710
PRNP
0.925 0.040 20 4699655 stop gained T/G snv 3
rs74315401
PRNP
0.683 0.320 20 4699525 missense variant C/T snv 32
rs28933385
PRNP
0.695 0.320 20 4699818 missense variant G/A snv 4.0E-06 25
rs1799990
PRNP
0.683 0.440 20 4699605 missense variant A/G snv 0.31 0.33 23