Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs755683317
TPTE
21 10567746 missense variant G/A;C snv 2.4E-05 3
rs778826879
MAPK3
16 30121948 missense variant C/G;T snv 1.2E-05; 8.0E-06 3
rs1227480017
RRM2
2 10122697 synonymous variant C/A snv 1
rs12613347
CASP10
2 201190589 intron variant C/T snv 0.19 1
rs143752852
MST1R ; LOC102724438
3 49902723 missense variant A/G snv 8.8E-05 5.6E-05 1
rs150423237
EGFR
7 55173087 missense variant G/A snv 2.1E-04 2.4E-04 1
rs16906079
TLR4
9 117712651 missense variant A/G snv 6.5E-04 4.3E-04 1
rs17429138
LOC107986169
3 189527804 intergenic variant A/G snv 0.26 1
rs199647144
NTRK1 ; INSRR
1 156842109 missense variant T/C;G snv 8.8E-05; 4.0E-06 1
rs3764221
CYP19A1
15 51296650 intron variant G/A;T snv 1
rs4396880
TP63
3 189638432 intron variant G/A snv 0.34 1
rs542027040
MIR4728 ; ERBB2
17 39724864 missense variant C/T snv 1.2E-05 1
rs736775
TNIP1
5 151029787 downstream gene variant T/C snv 0.56 1
rs750749 6 14141866 downstream gene variant T/C snv 0.27 1
rs779577244
LOC107984219 ; KIF5B
10 32017334 missense variant C/A snv 4.0E-06 1
rs782212015
CEACAM5
19 41721077 missense variant G/A snv 8.0E-06 2.1E-05 1
rs8038415
IGF1R
15 98956205 intron variant T/C snv 0.58 1
rs863225307
APC
5 112819077 stop gained C/T snv 1
rs9370729 6 14138061 downstream gene variant C/T snv 0.44 1
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs113488022
BRAF
0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490
rs121913377
BRAF
0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
rs397507444
MTHFR
0.405 0.880 1 11794407 missense variant T/G snv 306
rs4986790
TLR4
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs25487
XRCC1
0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205