Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1799752
ACE
0.677 0.480 17 63488529 intron variant -/TTTTTTTTTTTGAGACGGAGTCTCGCTCTGTCGCCCATACAGTCACTTTT delins 25
rs5186
AGTR1
0.630 0.560 3 148742201 3 prime UTR variant A/C snv 0.23 0.21 38
rs201106962
SNCA
0.851 0.080 4 89828156 missense variant A/C snv 8.0E-05 7.0E-05 5
rs63750231
PSEN1
0.689 0.160 14 73198100 missense variant A/C;G snv 23
rs767543900
MAPT
0.790 0.120 17 45971879 missense variant A/C;G snv 4.0E-06 10
rs770237371
ASPSCR1
0.827 0.160 17 81996616 missense variant A/C;G snv 4.0E-06; 1.2E-05 5
rs854560
PON1
0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 113
rs2306604
TFAM
0.827 0.080 10 58388932 intron variant A/C;G;T snv 5
rs2228145
IL6R
0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 57
rs3764435
ALDH1A1
0.827 0.120 9 72901960 intron variant A/C;T snv 5
rs9357347
LOC107986595
0.851 0.080 6 41182853 intergenic variant A/C;T snv 4
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1805087
MTR
0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 135
rs16944
IL1B
0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 92
rs334558
LOC107986119 ; GSK3B
0.701 0.320 3 120094435 upstream gene variant A/G snv 0.51 20
rs17125721
PSEN1
0.763 0.120 14 73206470 missense variant A/G snv 1.5E-02 1.5E-02 14
rs3093059
CRP
0.752 0.520 1 159715346 upstream gene variant A/G snv 0.13 11
rs956572
BCL2
0.742 0.280 18 63153338 intron variant A/G snv 0.65 11
rs5930
MIR6886 ; LDLR
0.827 0.200 19 11113589 synonymous variant A/G snv 0.63 0.66 8
rs74315413
PRNP
0.807 0.160 20 4699780 missense variant A/G snv 8
rs63751037
PSEN1
0.790 0.080 14 73173642 missense variant A/G snv 7
rs1401663578
ACE
0.882 0.120 17 63483037 missense variant A/G snv 1.4E-05 4
rs910080
PDYN ; PDYN-AS1
0.851 0.120 20 1979580 3 prime UTR variant A/G snv 0.35 4
rs2235751
PDYN-AS1 ; PDYN
0.882 0.120 20 1989288 intron variant A/G snv 0.40 3
rs2420616
GRK5
0.882 0.080 10 119316984 intron variant A/G snv 0.69 3