Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs750749 6 14141866 downstream gene variant T/C snv 0.27 1
rs9370729 6 14138061 downstream gene variant C/T snv 0.44 1
rs863225307
APC
5 112819077 stop gained C/T snv 1
rs12613347
CASP10
2 201190589 intron variant C/T snv 0.19 1
rs782212015
CEACAM5
19 41721077 missense variant G/A snv 8.0E-06 2.1E-05 1
rs3764221
CYP19A1
15 51296650 intron variant G/A;T snv 1
rs150423237
EGFR
7 55173087 missense variant G/A snv 2.1E-04 2.4E-04 1
rs8038415
IGF1R
15 98956205 intron variant T/C snv 0.58 1
rs779577244
LOC107984219 ; KIF5B
10 32017334 missense variant C/A snv 4.0E-06 1
rs17429138
LOC107986169
3 189527804 intergenic variant A/G snv 0.26 1
rs542027040
MIR4728 ; ERBB2
17 39724864 missense variant C/T snv 1.2E-05 1
rs143752852
MST1R ; LOC102724438
3 49902723 missense variant A/G snv 8.8E-05 5.6E-05 1
rs199647144
NTRK1 ; INSRR
1 156842109 missense variant T/C;G snv 8.8E-05; 4.0E-06 1
rs1227480017
RRM2
2 10122697 synonymous variant C/A snv 1
rs16906079
TLR4
9 117712651 missense variant A/G snv 6.5E-04 4.3E-04 1
rs736775
TNIP1
5 151029787 downstream gene variant T/C snv 0.56 1
rs4396880
TP63
3 189638432 intron variant G/A snv 0.34 1
rs10503380 1.000 0.080 8 9552985 upstream gene variant C/T snv 0.25 2
rs11991621 1.000 0.080 8 9549072 intergenic variant C/T snv 0.18 2
rs6601328 1.000 0.080 8 9545693 regulatory region variant G/A;C snv 2
rs766779326
ESR1
1.000 0.040 6 151944344 missense variant C/T snv 4.0E-06 7.0E-06 2
rs586339
KDM4A
1.000 0.080 1 43671586 missense variant C/A;G;T snv 0.70 0.78 2
rs764664272
MMP2
1.000 0.120 16 55484060 missense variant A/G snv 1.2E-05 7.0E-06 2
rs11466345
TGFB1
1.000 0.080 19 41337556 intron variant T/C snv 0.12 2
rs12541709
TNKS
1.000 0.080 8 9751081 intron variant C/G snv 0.29 2