Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2647045 6 32700323 TF binding site variant G/A snv 0.27 1
rs4530903 6 32614112 intergenic variant C/T snv 0.10 1
rs273429
LOC105375763
8 131467654 intergenic variant C/T snv 0.43 1
rs12289961
OR10Q2P
11 58292720 non coding transcript exon variant C/T snv 0.28 1
rs948562
ZFP91-CNTF ; ZFP91
11 58580292 intron variant A/G snv 0.15 1
rs6773854
LOC105374265
1.000 0.120 3 187931631 downstream gene variant T/C snv 0.23 2
rs11466782
ADAM19
0.925 0.120 5 157494947 intron variant A/G snv 0.10 3
rs2466571
CD46
0.925 0.120 1 207766701 intron variant G/T snv 0.46 3
rs1802710
DLK1
14 100734308 synonymous variant T/A;C snv 0.63 3
rs867329357
ERCC5 ; BIVM-ERCC5
0.925 0.120 13 102872275 missense variant G/A snv 4.0E-06 4.9E-05 3
rs1057519833
EZH2
0.925 0.120 7 148809375 missense variant G/C snv 3
rs10494879
IL19
0.925 0.120 1 206778859 intron variant C/A;G snv 0.36 3
rs707824
LOC101928354
0.925 0.120 6 14636732 intergenic variant T/C snv 0.74 3
rs1257715362
MAPK10 ; ARHGAP24
0.925 0.120 4 85995065 missense variant A/G snv 7.0E-06 3
rs1042752
POU2AF1
0.925 0.120 11 111352386 3 prime UTR variant A/G snv 0.39 3
rs869312777
PTEN
0.925 0.120 10 87933245 missense variant C/G snv 3
rs708486
PTGDR
0.925 0.120 14 52274253 intron variant A/G snv 0.35 3
rs138228187
TIRAP
0.925 0.120 11 126292650 missense variant C/T snv 4.0E-05 1.4E-05 3
rs867830180
TNFRSF6B ; RTEL1 ; RTEL1-TNFRSF6B
0.925 0.120 20 63695147 missense variant G/A;T snv 3
rs1555525126
TP53
0.925 0.120 17 7673749 missense variant T/C snv 3
rs1351687973
TP73
0.925 0.120 1 3731497 missense variant G/A snv 1.6E-05 3
rs535311760
TP73
0.925 0.120 1 3730979 missense variant G/A snv 1.2E-05; 8.2E-06 3
rs2621416 0.882 0.280 6 32774091 intergenic variant T/C snv 0.26 4
rs751837
CDC42BPB
0.882 0.120 14 103018488 intron variant T/C snv 0.23 4
rs10190751
CFLAR-AS1 ; CFLAR
0.882 0.120 2 201141373 splice acceptor variant G/A snv 0.18 0.26 4