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
rs10052657
PDE4D
0.807 0.120 5 59111944 intron variant C/A snv 0.17 7
rs10074991
PRKAA1
0.851 0.120 5 40790449 intron variant G/A snv 0.31 7
rs10421916
INSL3
0.925 0.080 19 17818178 intron variant A/G snv 0.69 2
rs10474606
THBS4
0.925 0.080 5 80057163 intron variant G/A snv 0.28 2
rs10499563
STEAP1B
0.807 0.120 7 22720869 intron variant T/C snv 0.21 7
rs10505477
CASC8 ; PCAT1 ; POU5F1B
0.658 0.400 8 127395198 intron variant A/G snv 0.40 31
rs10509670
PLCE1
0.851 0.080 10 94308190 intron variant A/G snv 0.30 5
rs10511729
LOC101929563
0.742 0.240 9 23557229 intron variant T/G snv 0.35 11
rs10512263
TGFBR1
0.851 0.120 9 99123789 intron variant T/C snv 6.5E-02 4
rs10680577
RAB4B-EGLN2 ; EGLN2
0.776 0.160 19 40798690 intron variant -/TACT delins 10
rs10739971
MIRLET7A1 ; MIRLET7F1
0.882 0.080 9 94175398 intron variant G/A;C snv 5
rs11066280
HECTD4
0.742 0.280 12 112379979 intron variant T/A snv 7.0E-03 27
rs11134527
MIR218-2 ; SLIT3
0.677 0.400 5 168768351 intron variant G/A snv 0.25 24
rs11187842
PLCE1
0.925 0.080 10 94292754 intron variant C/T snv 7.8E-02 5
rs1143633
IL1B
0.752 0.280 2 112832890 intron variant C/G;T snv 11
rs11536878
TLR4
0.827 0.240 9 117709275 intron variant C/A snv 9.5E-02 5
rs11564475
CTNNB1
0.882 0.080 3 41238542 intron variant A/G snv 3.7E-02 3
rs115797771
KLF5
0.807 0.080 13 73064505 intron variant A/C snv 5.8E-02 6
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
rs1179251
IL22 ; LOC105369818
0.763 0.320 12 68251271 intron variant C/G snv 0.18 14
rs11869286
STARD3
0.925 0.080 17 39657603 intron variant G/C snv 0.52 4