Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9350
EXO1
0.742 0.240 1 241885372 missense variant C/T snv 0.21 0.19 16
rs74315364
RNASEL
0.732 0.200 1 182586014 stop gained C/A snv 3.6E-03; 4.0E-06 3.3E-03 13
rs201765376
MTR
0.732 0.360 1 236838504 synonymous variant C/T snv 1.6E-05 1.4E-05 12
rs2536
MTOR
0.776 0.240 1 11106656 3 prime UTR variant T/C snv 5.8E-02 11
rs7483
GSTM3 ; GSTM5
0.742 0.320 1 109737079 missense variant C/T snv 4.0E-06; 0.35 0.26 11
rs1380576
MDM4
0.763 0.240 1 204519150 intron variant G/C snv 0.57 10
rs627928
RNASEL
0.790 0.080 1 182582202 missense variant A/C snv 0.54 0.49 10
rs1052576
CASP9
0.807 0.200 1 15506048 missense variant T/A;C snv 0.53 9
rs689470
PTGS2
0.776 0.240 1 186671926 3 prime UTR variant G/A;C;T snv 9
rs1012477
PER3
0.827 0.160 1 7798075 intron variant G/C snv 0.16 8
rs1883965
MTOR
0.807 0.160 1 11262099 intron variant A/G snv 0.63 8
rs4645978
CASP9 ; DNAJC16
0.827 0.120 1 15525539 intron variant C/A;T snv 8
rs748500299
PTGS2
0.790 0.200 1 186675960 missense variant T/A;C snv 4.0E-06; 4.0E-06 8
rs689465
PTGS2 ; PACERR
0.851 0.200 1 186681714 upstream gene variant T/C snv 0.14 7
rs2745557
PACERR ; PTGS2
0.807 0.200 1 186680089 intron variant A/G snv 0.83 6
rs3024496
IL10
0.827 0.200 1 206768519 3 prime UTR variant A/G snv 0.43 6
rs5013329
NSUN4
0.827 0.160 1 46349419 intron variant C/T snv 0.23 6
rs1034528
MTOR ; ANGPTL7
0.882 0.120 1 11189075 intron variant G/C snv 0.30 5
rs55829688
SNORD77 ; SNORA103 ; ZBTB37 ; SNORD76 ; SNORD74 ; SNORD75 ; GAS5
0.827 0.200 1 173868168 5 prime UTR variant T/C;G snv 5
rs1047303
HSD3B1
0.851 0.120 1 119514623 missense variant C/A snv 0.75 4
rs11102001
GSTM5 ; EPS8L3
0.925 0.080 1 109757069 missense variant G/A snv 9.4E-02 0.16 4
rs1360698171
RNASEL
0.851 0.080 1 182584103 missense variant T/C snv 4
rs17036508
MTOR ; ANGPTL7
0.925 0.080 1 11195977 3 prime UTR variant T/C snv 9.0E-02 4
rs2297480
FDPS
0.851 0.280 1 155309691 non coding transcript exon variant T/G snv 0.28 4
rs3753793
CCN1 ; DDAH1
0.851 0.240 1 85580205 upstream gene variant A/C snv 0.26 4