Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1256061
ESR2
14 64236875 intron variant G/A;T snv 5
rs1018379423
EPHB2
1 22907986 missense variant G/T snv 4.0E-06 2.1E-05 4
rs1174029586
CANX
5 179705693 missense variant G/C snv 8.2E-06 1
rs1242640031
CRK
17 1456106 missense variant G/C snv 1
rs8021944
ESR2 ; SYNE2
14 64212580 intron variant T/G snv 5.6E-02 1
rs947996134
CCDC8
19 46412799 missense variant G/C snv 1.2E-05 2.1E-05 1
rs1052559
KLC3 ; ERCC2
1.000 0.040 19 45351661 stop gained T/A;G snv 2
rs759404153
EPHB2
1.000 0.040 1 22910452 missense variant T/A;G snv 2.8E-05; 4.0E-06 2
rs1057519783
ALK
0.851 0.080 2 29220747 missense variant C/T snv 10
rs1458974438
STK11
0.807 0.080 19 1206957 missense variant G/A snv 9
rs772399455
MYCNOS ; MYCN
0.851 0.080 2 15942096 missense variant G/A;C snv 4.0E-06 6
rs775514340
CILK1
0.882 0.080 6 53041202 missense variant T/A;C snv 4.0E-06 5
rs1192694481
MMP13
0.882 0.080 11 102955629 missense variant C/T snv 4.0E-06 4
rs12072037
MFSD2A
0.882 0.080 1 39954534 upstream gene variant C/A snv 6.1E-02 4
rs1238968510
MMP2
0.882 0.080 16 55479556 missense variant A/G;T snv 4.1E-06 2.1E-05 4
rs6808523
SATB1 ; TBC1D5
0.882 0.080 3 18430796 intron variant A/G snv 8.0E-02 4
rs112295309
SCRIB ; MIR937
1.000 0.080 8 143813896 missense variant T/C;G snv 6.1E-04 3
rs3743073
CHRNA3
0.807 0.120 15 78617197 intron variant G/T snv 0.61 11
rs199976573
ABCG2
0.925 0.120 4 88132618 missense variant C/T snv 6.4E-05 5.6E-05 4
rs10146204 1.000 0.120 14 64352051 non coding transcript exon variant G/A snv 0.45 2
rs16906252
MGMT
0.732 0.200 10 129467281 synonymous variant C/T snv 5.5E-02 5.1E-02 19
rs588765
CHRNA5
0.827 0.200 15 78573083 intron variant T/A;C snv 6
rs372043866
ERBB2
0.732 0.240 17 39727965 missense variant G/A;C;T snv 3.2E-05; 2.4E-05; 1.2E-05 18
rs587782329
TP53
0.677 0.280 17 7674217 missense variant C/A;G;T snv 23
rs121913369
BRAF
0.790 0.280 7 140753346 missense variant G/A;C snv 4.0E-06 12