Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10483639 1.000 0.040 14 54839739 downstream gene variant G/C snv 0.26 3
rs13361160 1.000 0.040 5 10169711 downstream gene variant T/C snv 0.34 2
rs6961071 1.000 0.120 7 156182007 downstream gene variant A/G;T snv 0.47 2
rs943552 1 156885826 downstream gene variant C/T snv 9.7E-02 2
rs1800629
TNF
0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 169
rs4073
CXCL8
0.566 0.800 4 73740307 upstream gene variant A/T snv 0.46 64
rs1799964
LTA ; LOC100287329 ; TNF
0.608 0.760 6 31574531 upstream gene variant T/C snv 0.19 47
rs1800587
IL1A
0.620 0.720 2 112785383 upstream gene variant G/A;C snv 0.32 43
rs6311
HTR2A
0.645 0.640 13 46897343 upstream gene variant C/T snv 0.40 41
rs1536309
MIR146B
0.851 0.160 10 102435445 upstream gene variant A/G snv 0.32 7
rs10166942
TRPM8
0.925 0.040 2 233916448 upstream gene variant T/C snv 0.40 4
rs17197936 0.925 0.040 13 37601702 upstream gene variant T/C snv 5.2E-02 3
rs2233409
NFKBIA
1.000 0.080 14 35405064 upstream gene variant G/A snv 0.19 3
rs12948783
RHBDF2
17 76503318 upstream gene variant G/A;C;T snv 1
rs1571138 1 46429969 upstream gene variant A/G snv 0.73 1
rs17289394 13 46899085 upstream gene variant G/A snv 0.33 1
rs2383515 1 186683820 upstream gene variant G/A;T snv 1
rs398655 13 33013514 upstream gene variant A/C snv 0.51 1
rs72520913
MMP3
11 102845217 upstream gene variant -/C;G ins 1
rs7335912 13 95015426 upstream gene variant A/G snv 0.16 1
rs4660928 1 46420268 TF binding site variant A/C snv 0.63 1
rs61751364
MECP2
0.882 0.120 X 154030944 frameshift variant CGGAT/- delins 4
rs11614913
HOXC6 ; MIR196A2
0.512 0.760 12 53991815 mature miRNA variant C/T snv 0.39 0.34 111
rs5275
PTGS2
0.583 0.560 1 186673926 3 prime UTR variant A/G;T snv 55
rs165599
ARVCF ; COMT
0.677 0.280 22 19969258 3 prime UTR variant G/A snv 0.56 27