Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6116477 20 4704015 downstream gene variant T/C snv 0.23 1
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
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
rs6052751
RPS4XP2
20 4664427 intron variant G/A;C snv 1
rs2756271
RPS4XP2 ; PRNP
20 4684616 intron variant A/G;T snv 1
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
rs4538475
BST1
1.000 0.040 4 15736314 intron variant A/G snv 0.24 2
rs9349407
CD2AP
1.000 0.080 6 47485642 intron variant G/C snv 0.23 2
rs766487967
NPRL3 ; MPG
1.000 0.120 16 85517 missense variant G/A snv 8.0E-06 5.6E-05 2
rs12734001
PPP1R12B
1.000 0.080 1 202421786 intron variant C/T snv 3.5E-05 2
rs267606980
PRNP
1.000 0.080 20 4699600 missense variant G/T snv 4.0E-06 2
rs372878791
PRNP
1.000 0.120 20 4699783 missense variant C/G;T snv 3.2E-05; 4.0E-05 2
rs6107516
PRNP
1.000 0.120 20 4696446 intron variant G/A snv 0.23 2
rs74315410
PRNP
1.000 0.120 20 4699612 missense variant G/T snv 4.0E-06 2
rs776593792
PRNP
1.000 0.120 20 4699827 missense variant G/A snv 1.6E-05 2.8E-05 2
rs1994090
SLC2A13
1.000 0.040 12 40034759 intron variant G/A;T snv 2
rs597668
BLOC1S3 ; MARK4
0.925 0.080 19 45205630 intron variant T/A;C;G snv 3
rs368821179
CARD14
0.925 0.160 17 80182758 missense variant T/C snv 8.0E-06 2.1E-05 3
rs12817488
CCDC62
1.000 0.040 12 122811747 intron variant G/A snv 0.39 3
rs1473972013
CYP4X1
0.925 0.160 1 47035911 missense variant G/A snv 7.0E-06 3