Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs412396 20 43657322 downstream gene variant C/G snv 0.77 2
rs2010963
VEGFA
0.542 0.840 6 43770613 5 prime UTR variant C/G snv 0.68 82
rs12953717
SMAD7
0.724 0.240 18 48927559 intron variant C/T snv 0.36 18
rs7987649
FLT1
0.925 0.080 13 28320278 intron variant A/G snv 0.35 4
rs6964824
PRKAG2
7 151654146 intron variant T/C snv 0.31 2
rs861539
KLC1 ; XRCC3
0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 104
rs1961177
CYP19A1
15 51332881 intron variant C/T snv 0.21 1
rs4725431
PRKAG2
7 151776093 intron variant T/C snv 0.19 2
rs4812219 20 60847915 intergenic variant C/T snv 0.13 1
rs17280262 14 96587587 upstream gene variant C/T snv 5.1E-02 1
rs56848936
SYMPK
0.776 0.080 19 45818249 intron variant A/G snv 1.9E-02 11
rs1801155
APC
0.649 0.440 5 112839514 missense variant T/A snv 8.0E-06; 2.0E-03 1.2E-03 42
rs35918369
EGFR
7 55205613 missense variant C/T snv 3.1E-04 3.3E-04 4
rs140516819
EGFR
7 55172999 missense variant A/C;G snv 4.0E-05 2.4E-04 4
rs587780053
PMS2
7 5977698 missense variant C/T snv 8.0E-06 1.4E-05 1
rs864622553
PMS2
7 5987540 missense variant C/G snv 1.2E-05 1.4E-05 1
rs1064793236
PMS2
7 5986802 missense variant C/T snv 7.0E-06 1
rs112431538
TP53
1.000 0.120 17 7673767 missense variant C/T snv 7.0E-06 4
rs121912665
TP53
1.000 0.120 17 7674965 missense variant G/A snv 2.4E-05 7.0E-06 7
rs768824654
MSH2
1.000 0.120 2 47403390 start lost A/G snv 7.0E-06 6
rs1219568637
EGFR
7 55143404 missense variant G/A snv 7.0E-06 2
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