Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1224426272
CIT
0.925 0.040 12 119869138 missense variant C/T snv 6
rs4409766
BORCS7-ASMT ; BORCS7
1.000 0.040 10 102856906 intron variant T/C snv 0.14 6
rs121917763
TH
0.925 0.040 11 2167896 missense variant A/G snv 1.2E-05 7.0E-06 5
rs4434553
TFR2
1.000 0.040 7 100642568 intron variant A/G snv 0.40 5
rs45539432
PINK1-AS ; PINK1
0.851 0.040 1 20649109 stop gained C/T snv 4.0E-05 3.5E-05 5
rs762472005
SACM1L
0.851 0.040 3 45722873 missense variant G/A snv 1.2E-05 7.0E-06 5
rs763222239
EIF4G1
0.827 0.040 3 184322862 missense variant G/A snv 4.0E-06 5
rs1060499619
SYNJ1
0.851 0.040 21 32681590 missense variant C/G snv 4
rs17563986
MAPT
1.000 0.040 17 45913906 intron variant A/G snv 0.14 4
rs1801334
PRKN
0.851 0.040 6 161360193 missense variant C/T snv 2.5E-02 2.5E-02 4
rs1991556
MAPT
1.000 0.040 17 46006036 intron variant G/A snv 0.14 4
rs368134308
PRKN
0.882 0.040 6 162443356 missense variant C/A;G;T snv 3.2E-05; 2.6E-04 4
rs466448
APP
0.925 0.040 21 26171790 intron variant A/C;G snv 4
rs71653619
PARK7
1.000 0.040 1 7970934 missense variant G/A snv 7.9E-03 7.0E-03 4
rs864309650
CHCHD2
0.851 0.040 7 56104344 missense variant G/A snv 4
rs10518765
UNC13C
1.000 0.040 15 54388434 intron variant A/C snv 0.16 3
rs1060501198
TP53
0.925 0.040 17 7674900 missense variant T/C;G snv 3
rs12720208
FGF20
0.925 0.040 8 16992890 3 prime UTR variant G/A snv 5.5E-02 3
rs12817488
CCDC62
1.000 0.040 12 122811747 intron variant G/A snv 0.39 3
rs1290141855
SLC6A2
1.000 0.040 16 55698539 missense variant T/C snv 4.0E-06 7.0E-06 3
rs1564282
GAK
1.000 0.040 4 858525 intron variant C/T snv 8.1E-02 3
rs1876829
LINC02210-CRHR1 ; MAPT-AS1 ; CRHR1
1.000 0.040 17 45834077 intron variant T/C snv 0.15 0.14 3
rs1981997
MAPT
1.000 0.040 17 45979401 non coding transcript exon variant G/A snv 0.14 3
rs200660418
LRRK2
1.000 0.040 12 40310449 missense variant C/A;G;T snv 3
rs2668692
KANSL1
1.000 0.040 17 46215654 intron variant G/A;T snv 3