Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1188539174
LRRK2
12 40232341 missense variant C/T snv 4.0E-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
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
rs1473972013
CYP4X1
0.925 0.160 1 47035911 missense variant G/A snv 7.0E-06 3
rs1292160648
PRNP
20 4699738 missense variant A/G snv 4.0E-06 7.0E-06 1
rs761807915
PRNP
0.925 0.120 20 4699824 missense variant G/A snv 4.0E-06 7.0E-06 4
rs368821179
CARD14
0.925 0.160 17 80182758 missense variant T/C snv 8.0E-06 2.1E-05 3
rs74315409
PRNP
0.742 0.240 20 4699915 missense variant T/G snv 6.0E-05 2.1E-05 13
rs74315407
PRNP
0.732 0.240 20 4699848 missense variant G/A snv 8.0E-06 2.1E-05 15
rs372805579
CARD14
0.851 0.200 17 80195302 missense variant G/A snv 2.4E-05 2.8E-05 5
rs1178466848
PRNP
0.925 0.120 20 4699785 missense variant G/A snv 2.8E-05 4
rs776593792
PRNP
1.000 0.120 20 4699827 missense variant G/A snv 1.6E-05 2.8E-05 2
rs751882709
PRNP
0.925 0.160 20 4699855 missense variant A/C snv 1.6E-05 2.8E-05 3
rs12734001
PPP1R12B
1.000 0.080 1 202421786 intron variant C/T snv 3.5E-05 2
rs74315412
PRNP
0.851 0.120 20 4699843 missense variant G/A snv 6.0E-05 3.5E-05 5
rs74315408
PRNP
0.752 0.280 20 4699758 missense variant G/A snv 6.4E-05 4.2E-05 16
rs766487967
NPRL3 ; MPG
1.000 0.120 16 85517 missense variant G/A snv 8.0E-06 5.6E-05 2
rs1800014
PRNP
0.776 0.200 20 4699875 missense variant G/A snv 8.0E-03 2.2E-03 11
rs16990018
PRNP
0.882 0.120 20 4699732 missense variant A/G snv 3.8E-03 1.6E-02 5
rs10994443
ANK3
1.000 0.040 10 60635760 intron variant G/A snv 0.11 2
rs1016726
CHN2
7 29316787 intron variant G/A snv 0.12 1
rs2075650
TOMM40
0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 45