Disease: Stomach Carcinoma
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10022537
PROM1
0.925 0.080 4 16075214 intron variant A/T snv 0.70 2
rs1002765
CHMP2B ; MIR4795
0.851 0.080 3 87227912 intron variant G/A;C snv 4
rs10052016
SLC6A3
0.925 0.080 5 1427996 intron variant A/G snv 0.22 2
rs10088390
SFRP1
0.925 0.080 8 41264249 3 prime UTR variant C/G snv 0.19 2
rs1011445550
TP53
0.925 0.080 17 7676391 missense variant G/C snv 2
rs10421916
INSL3
0.925 0.080 19 17818178 intron variant A/G snv 0.69 2
rs1044432
BTBD10
0.925 0.080 11 13388251 3 prime UTR variant A/T snv 0.16 2
rs10464867
OSGIN2 ; NBN
0.925 0.080 8 89933370 3 prime UTR variant C/T snv 3.0E-02 2
rs10474606
THBS4
0.925 0.080 5 80057163 intron variant G/A snv 0.28 2
rs10484761 0.807 0.080 6 40834522 intergenic variant T/C snv 0.31 7
rs10509670
PLCE1
0.851 0.080 10 94308190 intron variant A/G snv 0.30 5
rs1051690
INSR
0.851 0.080 19 7116952 3 prime UTR variant T/C snv 0.83 4
rs1062935
RPTOR ; LOC400627
0.925 0.080 17 80966057 3 prime UTR variant T/C snv 0.40 2
rs1064261
MTOR
0.925 0.080 1 11228701 missense variant G/A;T snv 0.75; 4.0E-06 3
rs10739971
MIRLET7A1 ; MIRLET7F1
0.882 0.080 9 94175398 intron variant G/A;C snv 5
rs10787498
CASP7
0.925 0.080 10 113729891 3 prime UTR variant T/G snv 0.38 2
rs11040869 0.925 0.080 11 1263382 downstream gene variant G/A snv 1.8E-02 2
rs11084490
AURKC
0.925 0.080 19 57231104 5 prime UTR variant G/A;C;T snv 0.87; 3.8E-05 2
rs11088680 0.925 0.080 21 13514758 upstream gene variant A/G snv 0.30 2
rs11133399
CLOCK
0.925 0.080 4 55547664 non coding transcript exon variant A/G snv 0.28 2
rs111638916
PSMD10
0.925 0.080 X 108084839 3 prime UTR variant G/A snv 3
rs11170877
COPZ1
0.925 0.080 12 54340505 start lost A/G snv 0.16 0.17 2
rs11187842
PLCE1
0.925 0.080 10 94292754 intron variant C/T snv 7.8E-02 5
rs112310158
MIR449B ; MIR449A ; CDC20B
0.925 0.080 5 55170550 non coding transcript exon variant G/A snv 1.7E-03 7.5E-03 2
rs1126760
FAM71E2 ; IL11
0.925 0.080 19 55364706 3 prime UTR variant G/A;C snv 2