Disease: Stomach Carcinoma
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10004195
TLR10
0.790 0.320 4 38783103 upstream gene variant T/A snv 0.29 8
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
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
rs10116253 0.851 0.120 9 117702042 upstream gene variant T/C snv 0.28 4
rs1016343
PCAT2 ; PCAT1 ; PRNCR1 ; CASC19
0.807 0.240 8 127081052 non coding transcript exon variant C/T snv 0.20 8
rs10421916
INSL3
0.925 0.080 19 17818178 intron variant A/G snv 0.69 2
rs10434
VEGFA
0.701 0.480 6 43785475 3 prime UTR variant A/G snv 0.59 17
rs1044432
BTBD10
0.925 0.080 11 13388251 3 prime UTR variant A/T snv 0.16 2
rs1045411
HMGB1
0.708 0.360 13 30459095 3 prime UTR variant C/T snv 0.20 18
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
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
rs1051690
INSR
0.851 0.080 19 7116952 3 prime UTR variant T/C snv 0.83 4
rs1053023
STAT3
0.882 0.120 17 42313598 3 prime UTR variant T/A;C snv 4
rs1057317
TLR4
0.827 0.160 9 117715764 3 prime UTR variant C/A snv 5