Source: BEFREE ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1057519861
EGFR ; EGFR-AS1
0.776 0.080 7 55181398 missense variant T/A snv 15
rs1057519783
ALK
0.851 0.080 2 29220747 missense variant C/T snv 9
rs10937405
TP63
0.807 0.080 3 189665394 intron variant C/T snv 0.38 9
rs1458974438
STK11
0.807 0.080 19 1206957 missense variant G/A snv 9
rs6183
GHR
0.827 0.080 5 42718990 missense variant C/A snv 2.3E-03 7.4E-04 8
rs146795390
EGFR
0.827 0.080 7 55191776 missense variant G/A snv 8.0E-06 7.0E-06 7
rs1057519784
ALK
0.827 0.080 2 29220765 missense variant G/T snv 6
rs12894467
MIR300 ; MIR1185-1
0.807 0.080 14 101041390 non coding transcript exon variant C/T snv 0.51 0.50 6
rs1389500636
EGFR
0.827 0.080 7 55156796 missense variant G/A snv 6
rs171140
ERCC2
0.807 0.080 19 45361744 non coding transcript exon variant C/A snv 0.58 0.64 6
rs2233947
PSORS1C2 ; PSORS1C1
0.851 0.080 6 31139278 non coding transcript exon variant C/T snv 9.3E-03 6
rs2352028
GPC5
0.851 0.080 13 91792975 intron variant C/G;T snv 6
rs2564978
CD55
0.827 0.080 1 207321071 upstream gene variant T/C snv 0.77 6
rs2835267
SETD4 ; LOC100133286
0.827 0.080 21 36074727 intron variant T/C snv 0.63 6
rs4513061
AGBL1
0.807 0.080 15 86428401 intron variant G/A;T snv 6
rs6495309
CHRNB4 ; CHRNA3
0.807 0.080 15 78622903 upstream gene variant C/A;T snv 6
rs767935771
AXL
0.827 0.080 19 41259690 missense variant T/C snv 1.6E-05 5.6E-05 6
rs772399455
MYCNOS ; MYCN
0.851 0.080 2 15942096 missense variant G/A;C snv 4.0E-06 6
rs78768932
PXN
0.882 0.080 12 120222977 missense variant C/G;T snv 5.4E-03 5.4E-03 6
rs9895829
TP53
0.807 0.080 17 7675361 5 prime UTR variant A/G snv 7.4E-02 6
rs10254120
PMS2
0.851 0.080 7 6005996 missense variant C/A;G;T snv 7.2E-02 5
rs1026411
LOC105375751 ; PCAT1
0.827 0.080 8 127014165 intron variant G/A;C snv 0.25 5
rs1057519729
MAP2K1
0.827 0.080 15 66435113 missense variant A/C snv 5
rs12587742
DCAF4
0.851 0.080 14 72926683 intron variant G/A snv 0.18 5
rs1275824108
CDKN3
0.851 0.080 14 54399922 missense variant A/G snv 7.0E-06 5