Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1562430
PCAT1 ; CASC8 ; CASC21 ; POU5F1B
0.807 0.160 8 127375606 intron variant T/C snv 0.41 2
rs1874564
LOC107986291 ; LOC105377294
0.925 0.080 4 76936952 intergenic variant G/A snv 0.58 2
rs2069837
IL6-AS1 ; IL6
0.724 0.520 7 22728408 intron variant A/C;G snv 2
rs4649295
PCNX2
0.925 0.080 1 233280792 intron variant T/C snv 0.60 2
rs6996585
NRG1
0.925 0.080 8 32543285 intron variant A/G snv 0.37 2
rs944289 0.742 0.200 14 36180040 upstream gene variant C/T snv 0.45 2
rs949963
IL1R1
0.925 0.160 2 102153326 intron variant C/T snv 0.22 2
rs9858271
LOC105377110
0.925 0.080 3 59559604 intron variant G/A snv 0.80 2
rs1057519695
NRAS
0.641 0.520 1 114713907 missense variant TT/CA;CC mnv 1
rs1057519834
NRAS
0.658 0.480 1 114713908 missense variant TG/CT mnv 1
rs1057519855
HRAS ; LRRC56
0.776 0.120 11 533873 missense variant CT/AC;TC mnv 1
rs1131691014
TP53
0.439 0.800 17 7676154 frameshift variant -/C ins 1
rs1143633
IL1B
0.752 0.280 2 112832890 intron variant C/G;T snv 1
rs11762469
BRAF
1.000 0.080 7 140914412 intron variant A/G;T snv 1
rs121913227
BRAF
0.653 0.320 7 140753336 missense variant AC/CT;TT mnv 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
rs1867277
PTCSC2 ; FOXE1
0.776 0.160 9 97853632 5 prime UTR variant A/G snv 0.63 1
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
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
rs368187
LOC105370452
0.925 0.080 14 36063370 non coding transcript exon variant G/A;C;T snv 1
rs3737787
TSTD1 ; USF1
0.763 0.280 1 161039733 3 prime UTR variant G/A snv 0.21 1
rs72753537
TRMO ; LOC112268051
1.000 0.080 9 97898464 intergenic variant T/C snv 9.4E-02 1