Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4975616 0.763 0.320 5 1315545 downstream gene variant G/A snv 0.51 5
rs6495309
CHRNB4 ; CHRNA3
0.807 0.080 15 78622903 upstream gene variant C/A;T snv 5
rs16969968
CHRNA5
0.653 0.360 15 78590583 missense variant G/A snv 0.26 0.24 4
rs2274223
PLCE1
0.620 0.400 10 94306584 missense variant A/G snv 0.28 0.31 4
rs3114020
ABCG2
0.882 0.200 4 88162514 intron variant T/C snv 0.40 3
rs1447295
CASC8
0.658 0.400 8 127472793 intron variant A/C;T snv 3
rs121913444
EGFR
0.724 0.160 7 55191831 missense variant T/A;C;G snv 3
rs28929495
EGFR
0.807 0.120 7 55174014 missense variant G/A;C;T snv 3
rs121913465
EGFR ; EGFR-AS1
0.763 0.160 7 55181312 missense variant G/T snv 3
rs6465657
LMTK2
0.807 0.280 7 98187015 intron variant C/T snv 0.41 0.37 3
rs217727
MRPL23 ; HOTS ; H19
0.641 0.480 11 1995678 non coding transcript exon variant G/A snv 0.20 3
rs3765524
PLCE1
0.724 0.320 10 94298541 missense variant C/T snv 0.27 0.31 3
rs12296850 0.925 0.080 12 100426307 downstream gene variant A/G snv 8.7E-02 2
rs121434592
AKT1
0.595 0.640 14 104780214 missense variant C/T snv 4.0E-06 2
rs121913377
BRAF
0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 2
rs2072671
CDA
0.752 0.280 1 20589208 missense variant A/C snv 0.28 0.25 2
rs2229094
LOC100287329 ; LTA
0.776 0.320 6 31572779 missense variant T/C snv 0.27 0.27 2
rs2239704
LTA ; LOC100287329
0.732 0.320 6 31572364 5 prime UTR variant A/C snv 0.64 2
rs909253
LTA ; LOC100287329
0.641 0.600 6 31572536 intron variant A/G;T snv 2
rs1799724
LTA ; TNF
0.600 0.680 6 31574705 upstream gene variant C/T snv 8.5E-02 2
rs16906252
MGMT
0.732 0.200 10 129467281 synonymous variant C/T snv 5.5E-02 5.1E-02 2
rs2736098
TERT
0.600 0.600 5 1293971 synonymous variant C/T snv 0.29 0.22 2
rs2070803
TRIM46
0.925 0.080 1 155185239 intron variant G/A snv 0.55 2
rs1057519696
ALK
1.000 0.040 2 29214054 missense variant C/T snv 1
rs2279574
DUSP6
0.827 0.120 12 89351700 missense variant C/A;T snv 0.52 1