Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs104893877
SNCA
0.614 0.360 4 89828149 missense variant C/T snv 59
rs1085307051
MEF2C-AS1 ; MEF2C
0.925 0.160 5 88883309 5 prime UTR variant GAGGAGGAGGAAGA/- del 5
rs302668
RAB38
0.925 0.120 11 88143743 intron variant T/C snv 0.28 2
rs4878104
DAPK1
0.851 0.120 9 87578076 intron variant C/T snv 0.40 4
rs4877365
DAPK1
0.851 0.120 9 87540777 intron variant G/A snv 0.28 4
rs981951447
RASA1
0.925 0.120 5 87268726 missense variant C/T snv 2
rs78268395
CHMP2B
1.000 0.120 3 87253740 missense variant G/A snv 1.5E-03 6.9E-03 1
rs72824905
PLCG2
0.827 0.200 16 81908423 missense variant C/G;T snv 5.2E-03 6
rs2255166
NDUFAF8 ; TEPSIN
1.000 0.120 17 81239762 non coding transcript exon variant T/C snv 0.37 1
rs1048775
LOC105371925 ; TEPSIN
1.000 0.120 17 81228529 3 prime UTR variant G/C snv 0.42 1
rs969413
CEP131
1.000 0.120 17 81222014 intron variant T/A snv 0.39 1
rs9319617
CEP131
1.000 0.120 17 81218646 intron variant T/C snv 0.47 1
rs2725391
CEP131
1.000 0.120 17 81218630 intron variant C/T snv 0.37 1
rs2659030
CEP131
1.000 0.120 17 81204174 intron variant G/A;T snv 0.36 1
rs906175
CEP131
1.000 0.120 17 81199662 non coding transcript exon variant C/T snv 0.37 1
rs7240419
ATP9B
1.000 0.120 18 79168989 intron variant G/A snv 0.24 1
rs1401496725
REG1A
0.925 0.120 2 79121657 missense variant C/G;T snv 8.0E-06; 8.0E-06 2
rs544706237
REG1A
0.851 0.120 2 79121649 missense variant A/G;T snv 8.0E-06; 5.2E-05 5
rs1205185774
AHSA1
0.882 0.120 14 77469161 missense variant C/T snv 4
rs6962939
COL28A1
1.000 0.120 7 7484595 intron variant T/A snv 5.4E-02 1
rs121909345
DCTN1
0.882 0.120 2 74363337 missense variant C/T snv 2.8E-05 2.1E-05 4
rs63750083
PSEN1
0.732 0.160 14 73219177 missense variant C/A;T snv 13
rs63751223
PSEN1
0.807 0.160 14 73219161 missense variant G/C snv 6
rs661
PSEN1
0.807 0.120 14 73217225 missense variant G/A;T snv 4.0E-06 6
rs1566650594
PSEN1
0.851 0.120 14 73206384 splice acceptor variant A/T snv 4