Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11072508 1.000 0.080 15 74770056 regulatory region variant C/T snv 0.43 2
rs1114167857
MSH2
1.000 0.080 2 47476442 missense variant T/C snv 2
rs1131620
LTBP4
1.000 0.080 19 40611963 missense variant A/G snv 0.44 0.47 2
rs113561019
OGG1
1.000 0.080 3 9756791 missense variant G/A;T snv 3.9E-03; 4.0E-06 2
rs1137188
KRAS
1.000 0.080 12 25206418 3 prime UTR variant G/A snv 0.49 2
rs11777210
KBTBD11
1.000 0.080 8 1979843 intron variant C/G;T snv 2
rs121913317
STK11
1.000 0.080 19 1220503 stop gained G/A;T snv 2
rs1374712964
MUTYH
1.000 0.080 1 45332028 missense variant T/C snv 2
rs1399685
LOC105373668 ; LINC01911
1.000 0.080 2 146870842 intron variant T/A snv 3.2E-02 2
rs1400826115
OGG1
1.000 0.080 3 9756770 missense variant A/G snv 4.0E-06 2
rs1420111973
TLR4
1.000 0.080 9 117712527 synonymous variant T/C snv 7.0E-06 2
rs2222722
LINC00472 ; MIR30A
1.000 0.080 6 71404009 intron variant G/A snv 0.29 2
rs2241716
TGFB1
1.000 0.080 19 41348181 intron variant C/T snv 4.0E-02 2
rs2279398
DOK3
1.000 0.080 5 177503768 3 prime UTR variant C/T snv 2.7E-02 2
rs2286455
PROM1
1.000 0.080 4 16018539 splice region variant C/T snv 0.14 9.9E-02 2
rs2336219
CD3EAP ; ERCC1
1.000 0.080 19 45409148 missense variant G/A snv 0.21 0.19 2
rs4975605
TERT
1.000 0.080 5 1275413 intron variant C/A snv 0.43 2
rs5789
PTGS1
1.000 0.080 9 122381694 missense variant C/A snv 1.8E-02 1.8E-02 2
rs63749982
MSH2
1.000 0.080 2 47475121 missense variant A/G snv 4.0E-06 2
rs63751113
MSH6 ; FBXO11
1.000 0.080 2 47800910 missense variant G/A snv 2
rs63751260
MSH2
1.000 0.080 2 47403309 missense variant G/A snv 8.8E-06 2
rs6475526 1.000 0.080 9 21242162 upstream gene variant C/T snv 0.33 2
rs6755196
ROCK2
1.000 0.080 2 11320199 intron variant A/G;T snv 2
rs743554
ITGB4 ; GALK1
1.000 0.080 17 75758167 intron variant G/A snv 0.14 0.17 2
rs756703787
EGFR
1.000 0.080 7 55191845 missense variant G/A snv 4.0E-06 2