Disease: Malignant neoplasm of stomach
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10074991
PRKAA1
0.851 0.120 5 40790449 intron variant G/A snv 0.31 7
rs12733285
ADIPOR1
0.776 0.120 1 202952912 intron variant C/T snv 0.26 12
rs13361707
PRKAA1
0.882 0.120 5 40791782 intron variant C/T snv 0.31 7
rs1342387
ADIPOR1
0.776 0.120 1 202945228 intron variant T/C snv 0.53 12
rs1447295
CASC8
0.658 0.400 8 127472793 intron variant A/C;T snv 29
rs154268
PRKAA1
0.925 0.080 5 40795766 intron variant C/T snv 0.69 3
rs1569686
DNMT3B
0.752 0.400 20 32779273 intron variant G/A;C;T snv 15
rs1800469
B9D2 ; TGFB1
0.547 0.760 19 41354391 intron variant A/G snv 0.69 78
rs1800795
IL6-AS1 ; IL6 ; STEAP1B
0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs1800896
IL19 ; IL10
0.507 0.800 1 206773552 intron variant T/C snv 0.41 113
rs184003
AGER
0.724 0.400 6 32182519 intron variant C/A snv 0.12 0.12 15
rs2279744
MDM2
0.605 0.640 12 68808800 intron variant T/G snv 0.31 48
rs230310
TRIT1
0.925 0.080 1 39842047 intron variant A/G;T snv 3
rs243865
MMP2
0.600 0.640 16 55477894 intron variant C/T snv 0.19 48
rs2808668
XPA
0.851 0.120 9 97690153 intron variant C/G;T snv 7
rs353639
CD44 ; SNORD164
0.851 0.120 11 35162817 intron variant T/G snv 0.32 5
rs3743073
CHRNA3
0.807 0.120 15 78617197 intron variant G/T snv 0.61 11
rs3790843
NR5A2
0.827 0.160 1 200041696 intron variant C/T snv 0.29 7
rs3807987
CAV1
0.732 0.280 7 116539780 intron variant G/A snv 7.6E-02 17
rs4648068
NFKB1
0.790 0.240 4 102597148 intron variant A/G snv 0.31 9
rs505922
ABO
0.689 0.520 9 133273813 intron variant C/T snv 34
rs5742612
LOC105369944 ; IGF1
0.752 0.440 12 102481086 intron variant A/G snv 5.6E-02 11
rs744166
STAT3
0.689 0.560 17 42362183 intron variant A/G snv 0.48 22
rs7804372
CAV1
0.716 0.320 7 116554174 intron variant T/A snv 0.27 19
rs7903146
TCF7L2
0.554 0.680 10 112998590 intron variant C/G;T snv 93