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
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
rs1062935
RPTOR ; LOC400627
0.925 0.080 17 80966057 3 prime UTR variant T/C snv 0.40 2
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
rs11170877
COPZ1
0.925 0.080 12 54340505 start lost A/G snv 0.16 0.17 2
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
rs112754928
SPOCD1
0.925 0.080 1 31815123 missense variant G/A;T snv 4.5E-03; 1.2E-05 2
rs1127687
CASP7
0.925 0.080 10 113730350 3 prime UTR variant G/A snv 0.23 2
rs1141023
TRIM59 ; TRIM59-IFT80
0.925 0.080 3 160439163 synonymous variant C/T snv 0.15 0.14 2
rs1165109290
SOD2
0.925 0.080 6 159692850 synonymous variant G/A snv 4.2E-06 2
rs11656976
TOB1 ; TOB1-AS1
0.925 0.080 17 50869478 intron variant T/A;C snv 2
rs11695471
DNMT3A
0.925 0.080 2 25234839 intron variant T/A;C snv 2
rs11944405
LAMTOR3
0.925 0.080 4 99878804 3 prime UTR variant T/C snv 0.28 2
rs12231393
COPZ1
0.925 0.080 12 54318989 intron variant T/C snv 0.14 2