Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10509125
ANK3
10 60167108 intron variant C/A snv 0.56 2
rs1016726
CHN2
7 29316787 intron variant G/A snv 0.12 1
rs1188539174
LRRK2
12 40232341 missense variant C/T snv 4.0E-06 1
rs1292160648
PRNP
20 4699738 missense variant A/G snv 4.0E-06 7.0E-06 1
rs2756271
RPS4XP2 ; PRNP
20 4684616 intron variant A/G;T snv 1
rs6052751
RPS4XP2
20 4664427 intron variant G/A;C snv 1
rs6116477 20 4704015 downstream gene variant T/C snv 0.23 1
rs747500244
PRNP
20 4699797 missense variant A/G snv 1.2E-05 1
rs768562045
PRNP
20 4699821 missense variant A/T snv 4.0E-06 1
rs775144659
PRNP
20 4699816 missense variant C/A snv 1
rs2075650
TOMM40
0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 45
rs74315401
PRNP
0.683 0.320 20 4699525 missense variant C/T snv 32
rs1799990
PRNP
0.683 0.440 20 4699605 missense variant A/G snv 0.31 0.33 23
rs28933385
PRNP
0.695 0.320 20 4699818 missense variant G/A snv 4.0E-06 25
rs74315407
PRNP
0.732 0.240 20 4699848 missense variant G/A snv 8.0E-06 2.1E-05 15
rs1990622 0.742 0.200 7 12244161 downstream gene variant A/G snv 0.52 16
rs74315409
PRNP
0.742 0.240 20 4699915 missense variant T/G snv 6.0E-05 2.1E-05 13
rs11136000
CLU
0.752 0.160 8 27607002 intron variant T/C snv 0.56 19
rs74315408
PRNP
0.752 0.280 20 4699758 missense variant G/A snv 6.4E-05 4.2E-05 16
rs3851179 0.752 0.280 11 86157598 downstream gene variant T/C snv 0.70 15
rs1800014
PRNP
0.776 0.200 20 4699875 missense variant G/A snv 8.0E-03 2.2E-03 11
rs3849942
C9orf72 ; LOC107987057
0.776 0.200 9 27543283 non coding transcript exon variant T/A;C snv 9
rs74315403
PRNP
0.790 0.200 20 4699752 missense variant G/A snv 10
rs3764650
ABCA7
0.790 0.200 19 1046521 intron variant T/G snv 0.14 9
rs74315413
PRNP
0.807 0.160 20 4699780 missense variant A/G snv 8