Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs751882709
PRNP
0.925 0.160 20 4699855 missense variant A/C snv 1.6E-05 2.8E-05 3
rs2075650
TOMM40
0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 45
rs1799990
PRNP
0.683 0.440 20 4699605 missense variant A/G snv 0.31 0.33 23
rs1990622 0.742 0.200 7 12244161 downstream gene variant A/G snv 0.52 16
rs74315413
PRNP
0.807 0.160 20 4699780 missense variant A/G snv 8
rs744373 0.851 0.160 2 127137039 downstream gene variant A/G snv 0.35 8
rs393152
LINC02210 ; LINC02210-CRHR1
0.851 0.160 17 45641777 non coding transcript exon variant A/G snv 0.18 0.29 7
rs16990018
PRNP
0.882 0.120 20 4699732 missense variant A/G snv 3.8E-03 1.6E-02 5
rs74315406
PRNP
0.851 0.160 20 4699870 missense variant A/G snv 5
rs74315411
PRNP
0.882 0.160 20 4699767 missense variant A/G snv 4
rs947211
LOC105371702
0.925 0.040 1 205783537 non coding transcript exon variant A/G snv 0.64 3
rs4538475
BST1
1.000 0.040 4 15736314 intron variant A/G snv 0.24 2
rs1292160648
PRNP
20 4699738 missense variant A/G snv 4.0E-06 7.0E-06 1
rs747500244
PRNP
20 4699797 missense variant A/G snv 1.2E-05 1
rs2756271
RPS4XP2 ; PRNP
20 4684616 intron variant A/G;T snv 1
rs768562045
PRNP
20 4699821 missense variant A/T snv 4.0E-06 1
rs3865444
CD33
0.851 0.160 19 51224706 upstream gene variant C/A snv 0.25 8
rs398122414
PRNP
0.925 0.120 20 4699898 stop gained C/A snv 3
rs10509125
ANK3
10 60167108 intron variant C/A snv 0.56 2
rs775144659
PRNP
20 4699816 missense variant C/A snv 1
rs11538758
PRNP
0.882 0.160 20 4699534 missense variant C/A;T snv 8
rs74315414
PRNP
0.882 0.200 20 4699533 missense variant C/A;T snv 4.0E-06 5
rs2814707
LOC112268043 ; C9orf72 ; LOC107987057
0.882 0.120 9 27536399 non coding transcript exon variant C/G;T snv 4
rs372878791
PRNP
1.000 0.120 20 4699783 missense variant C/G;T snv 3.2E-05; 4.0E-05 2
rs74315401
PRNP
0.683 0.320 20 4699525 missense variant C/T snv 32