Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs769696078
EGFR
0.925 0.040 7 55154128 missense variant G/A snv 3
rs1249080185
EPHB2
0.882 0.080 1 22784698 missense variant G/A snv 3
rs879254044
MSH2
0.925 0.040 2 47475148 missense variant G/A;C;T snv 3
rs1057519913
MTOR
0.925 0.120 1 11157172 missense variant G/C snv 3
rs12645561
NEIL3
0.882 0.120 4 177339718 intron variant C/A;T snv 3
rs2033214
RBBP6
0.882 0.040 16 24566199 intron variant T/G snv 0.14 3
rs144551722 0.851 0.040 X 43632629 intergenic variant G/A snv 0.13 4
rs75061358 0.882 0.040 7 54848587 intergenic variant T/C;G snv 4
rs1320938886
BLZF1
0.851 0.040 1 169376605 missense variant T/G snv 4.0E-06 4
rs757066045
CDKN2A
0.882 0.040 9 21974725 missense variant C/T snv 8.2E-06 4
rs2017309
CHEK2
0.851 0.040 22 28735438 intron variant T/A snv 0.23 4
rs1029044314
DDR1
0.851 0.040 6 30898095 missense variant G/A snv 4
rs59060240
EGFR
0.882 0.040 7 55080369 intron variant AA/-;A;AAA;AAAA;AAAAAAAAAAA delins 4
rs723527
EGFR
0.882 0.040 7 55067179 intron variant A/G snv 0.53 4
rs1801591
ETFA
0.882 0.040 15 76286421 missense variant G/A snv 7.4E-02 6.4E-02 4
rs1306185959
FGFR1
0.851 0.040 8 38429805 missense variant T/C snv 7.0E-06 4
rs375391381
FRMD5
0.851 0.040 15 43883735 missense variant C/T snv 8.0E-06 1.4E-05 4
rs760090729
H3C10
0.851 0.040 6 27810468 missense variant G/A snv 4
rs866960721
H3C4
0.851 0.040 6 26196856 missense variant C/G;T snv 4.0E-06 4
rs1415342243
H3C6
0.851 0.040 6 26225549 missense variant G/A snv 4.0E-06 4
rs10852606
HEATR3
0.882 0.040 16 50094961 intron variant T/A;C snv 4
rs1381537616
HOXA10 ; HOXA9 ; HOXA10-HOXA9
0.851 0.040 7 27174132 missense variant C/T snv 4
rs12230172
LOC105369844
0.882 0.040 12 75848895 intron variant A/G snv 0.48 4
rs11233250
MIR4300HG
0.882 0.040 11 82685972 intron variant C/T snv 0.11 4
rs766265850
MIR4640 ; DDR1
0.851 0.040 6 30889239 missense variant G/A snv 8.1E-06 7.0E-06 4