Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs967461896
TP53
0.724 0.240 17 7675086 missense variant A/C;G;T snv 16
rs909253
LTA ; LOC100287329
0.641 0.600 6 31572536 intron variant A/G;T snv 2
rs876658657
MLH1
0.677 0.280 3 37020356 missense variant A/G snv 4.0E-06 1
rs79184941
FGFR2
0.617 0.600 10 121520163 missense variant G/A;C snv 5.6E-05; 4.0E-06 18
rs762846821
TP53
0.614 0.320 17 7675151 missense variant C/A;T snv 8.0E-06 1
rs6495309
CHRNB4 ; CHRNA3
0.807 0.080 15 78622903 upstream gene variant C/A;T snv 5
rs6465657
LMTK2
0.807 0.280 7 98187015 intron variant C/T snv 0.41 0.37 3
rs587782289
TP53
0.752 0.240 17 7674257 missense variant A/C;G;T snv 12
rs505922
ABO
0.689 0.520 9 133273813 intron variant C/T snv 19
rs4986790
TLR4
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 6
rs4977756
CDKN2B-AS1
0.683 0.440 9 22068653 intron variant G/A snv 0.64 7
rs4975616 0.763 0.320 5 1315545 downstream gene variant G/A snv 0.51 5
rs4072037
MUC1
0.732 0.240 1 155192276 splice acceptor variant C/A;T snv 0.59 7
rs401681
CLPTM1L
0.620 0.640 5 1321972 intron variant C/T snv 0.48 17
rs397517108
EGFR ; EGFR-AS1
0.790 0.120 7 55181312 missense variant GC/TT mnv 1
rs3811047
IL37
0.807 0.400 2 112913833 missense variant A/G snv 0.71 0.60 1
rs3765524
PLCE1
0.724 0.320 10 94298541 missense variant C/T snv 0.27 0.31 3
rs3114020
ABCG2
0.882 0.200 4 88162514 intron variant T/C snv 0.40 3
rs28934575
TP53
0.641 0.400 17 7674230 missense variant C/A;G;T snv 25
rs28929495
EGFR
0.807 0.120 7 55174014 missense variant G/A;C;T snv 3
rs2853677
TERT
0.724 0.240 5 1287079 3 prime UTR variant G/A snv 0.63 6
rs2853676
TERT
0.667 0.560 5 1288432 intron variant T/A;C snv 7
rs2853669
TERT
0.649 0.320 5 1295234 upstream gene variant A/G snv 0.25 1
rs2736100
TERT
0.550 0.880 5 1286401 3 prime UTR variant C/A snv 0.52 16
rs2736098
TERT
0.600 0.600 5 1293971 synonymous variant C/T snv 0.29 0.22 2