Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs104893875
SNCA
0.742 0.120 4 89828170 missense variant C/T snv 4.0E-06 13
rs2200733 0.752 0.240 4 110789013 intergenic variant C/T snv 0.18 12
rs11931074
SNCA ; LOC105377329
0.851 0.080 4 89718364 intron variant G/A;C;T snv 7
rs201106962
SNCA
0.851 0.080 4 89828156 missense variant A/C snv 8.0E-05 7.0E-05 5
rs223331
CISD2
0.851 0.160 4 102872408 intron variant T/A;C snv 5
rs223330
CISD2
0.851 0.160 4 102872502 intron variant T/A;C snv 4
rs17070145
WWC1
0.790 0.120 5 168418786 intron variant C/T snv 0.43 10
rs104893941
MRNIP ; SQSTM1
0.776 0.200 5 179836445 missense variant C/T snv 9.8E-04 1.3E-03 9
rs6347
SLC6A3
0.851 0.080 5 1411297 synonymous variant T/C snv 0.23 0.32 4
rs2070600
AGER
0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 82
rs1799724
LTA ; TNF
0.600 0.680 6 31574705 upstream gene variant C/T snv 8.5E-02 47
rs75932628
LOC105375056 ; TREM2
0.662 0.480 6 41161514 missense variant C/A;T snv 6.8E-05; 2.6E-03 28
rs1801132
ESR1
0.689 0.320 6 151944387 synonymous variant G/C snv 0.73 0.80 22
rs104894002
LOC105375056 ; TREM2
0.790 0.320 6 41161557 stop gained G/A snv 2.0E-05 2.1E-05 7
rs201258663
LOC105375056 ; TREM2
0.807 0.320 6 41161457 missense variant G/A snv 5.6E-05 4.9E-05 6
rs797044603
TREM2 ; LOC105375056
0.827 0.320 6 41161541 missense variant T/C snv 4.0E-06 5
rs1801474
PRKN
0.851 0.080 6 162201165 missense variant C/T snv 7.1E-02 5.3E-02 4
rs9357347
LOC107986595
0.851 0.080 6 41182853 intergenic variant A/C;T snv 4
rs766647311
TREML1 ; LOC105375056 ; TREM2
0.882 0.080 6 41159841 missense variant C/A;T snv 4.0E-06; 4.0E-06 3
rs9397456
ESR1
0.882 0.160 6 151926017 intron variant A/G;T snv 3
rs950530102
DST
0.882 0.160 6 56704357 missense variant C/T snv 3
rs1884049
ESR1
0.925 0.080 6 151966232 intron variant T/C snv 0.75 2
rs1799983
NOS3
0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs662
PON1
0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 157
rs854560
PON1
0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 113