Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121913407
CTNNB1
0.763 0.240 3 41224645 missense variant T/C;G snv 10
rs121913529
KRAS
0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 21
rs12990503
DIRC3
0.925 0.080 2 217429494 intron variant C/G snv 0.64 2
rs13181
KLC3 ; ERCC2
0.487 0.760 19 45351661 stop gained T/A;G snv 4.0E-06; 0.32 1
rs1420106
IL18RAP
0.851 0.200 2 102418584 upstream gene variant A/G snv 0.78 1
rs1443434
FOXE1
0.851 0.080 9 97855197 3 prime UTR variant G/T snv 0.63 1
rs1447295
CASC8
0.658 0.400 8 127472793 intron variant A/C;T snv 3
rs1562430
PCAT1 ; CASC8 ; CASC21 ; POU5F1B
0.807 0.160 8 127375606 intron variant T/C snv 0.41 2
rs1566734
PTPRJ
0.807 0.120 11 48123823 missense variant A/C snv 0.17 0.15 2
rs17879961
CHEK2
0.597 0.480 22 28725099 missense variant A/C;G snv 4.1E-03 15
rs1800682
ACTA2 ; FAS
0.637 0.440 10 88990206 non coding transcript exon variant A/G snv 0.54 7
rs1801516
ATM
0.627 0.400 11 108304735 missense variant G/A snv 0.11 0.11 3
rs1867277
PTCSC2 ; FOXE1
0.776 0.160 9 97853632 5 prime UTR variant A/G snv 0.63 1
rs1874564
LOC107986291 ; LOC105377294
0.925 0.080 4 76936952 intergenic variant G/A snv 0.58 2
rs2066827
GPR19 ; CDKN1B
0.695 0.320 12 12718165 missense variant T/A;C;G snv 1.6E-04; 1.6E-05; 0.26 1
rs2069837
IL6-AS1 ; IL6
0.724 0.520 7 22728408 intron variant A/C;G snv 2
rs2107538
LOC105371744 ; CCL5
0.763 0.360 17 35880776 5 prime UTR variant C/T snv 0.27 1
rs2279744
MDM2
0.605 0.640 12 68808800 intron variant T/G snv 0.31 1
rs231775
CTLA4
0.504 0.720 2 203867991 missense variant A/G;T snv 0.42; 4.0E-06 1
rs2439302
NRG1
0.776 0.200 8 32574851 intron variant G/C snv 0.54 1
rs2516839
USF1
0.732 0.320 1 161043331 5 prime UTR variant C/T snv 0.49 1
rs2622590
XKR4
0.925 0.080 8 55445714 intron variant G/A snv 0.15 3
rs2736098
TERT
0.600 0.600 5 1293971 synonymous variant C/T snv 0.29 0.22 2
rs2736100
TERT
0.550 0.880 5 1286401 3 prime UTR variant C/A snv 0.52 16
rs28933406
LRRC56 ; HRAS
0.667 0.480 11 533875 missense variant G/C;T snv 17