Source: CURATED

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs104886003
rs104886003
0.562 0.440 3 179218303 missense variant G/A;C snv 4.0E-06
CUI: C0038356
Disease: Stomach Neoplasms
Stomach Neoplasms
0.700 0
dbSNP: rs1057519044
rs1057519044
0.752 0.440 10 121517390 missense variant C/T snv
CUI: C0038356
Disease: Stomach Neoplasms
Stomach Neoplasms
0.700 0
dbSNP: rs121908382
rs121908382
1.000 0.080 1 45331530 missense variant G/A snv
CUI: C0038356
Disease: Stomach Neoplasms
Stomach Neoplasms
0.700 0
dbSNP: rs121908383
rs121908383
1.000 0.080 1 45331502 missense variant T/C snv
CUI: C0038356
Disease: Stomach Neoplasms
Stomach Neoplasms
0.700 0
dbSNP: rs121909144
rs121909144
10 3781852 missense variant G/A;T snv
CUI: C0038356
Disease: Stomach Neoplasms
Stomach Neoplasms
0.700 0
dbSNP: rs121909775
rs121909775
1.000 0.120 2 201205929 stop gained C/A;T snv 4.0E-06
CUI: C0038356
Disease: Stomach Neoplasms
Stomach Neoplasms
0.700 0
dbSNP: rs121909776
rs121909776
1.000 0.080 2 201187798 missense variant T/C snv 1.2E-04 2.8E-05
CUI: C0038356
Disease: Stomach Neoplasms
Stomach Neoplasms
0.700 0
dbSNP: rs121912469
rs121912469
1.000 0.080 5 132489457 missense variant T/A snv
CUI: C0038356
Disease: Stomach Neoplasms
Stomach Neoplasms
0.700 0
dbSNP: rs121913279
rs121913279
0.526 0.560 3 179234297 missense variant A/G;T snv 4.0E-06; 4.0E-06
CUI: C0038356
Disease: Stomach Neoplasms
Stomach Neoplasms
0.700 0
dbSNP: rs121913281
rs121913281
0.623 0.520 3 179234296 missense variant C/T snv
CUI: C0038356
Disease: Stomach Neoplasms
Stomach Neoplasms
0.700 0
dbSNP: rs121913478
rs121913478
0.708 0.640 10 121515280 missense variant T/C snv
CUI: C0038356
Disease: Stomach Neoplasms
Stomach Neoplasms
0.700 0
dbSNP: rs121913530
rs121913530
0.583 0.640 12 25245351 missense variant C/A;G;T snv
CUI: C0038356
Disease: Stomach Neoplasms
Stomach Neoplasms
0.700 0
dbSNP: rs121918487
rs121918487
0.716 0.440 10 121517378 missense variant C/A;G;T snv
CUI: C0038356
Disease: Stomach Neoplasms
Stomach Neoplasms
0.700 0
dbSNP: rs121918491
rs121918491
0.716 0.440 10 121517371 synonymous variant C/T snv 4.0E-06
CUI: C0038356
Disease: Stomach Neoplasms
Stomach Neoplasms
0.700 0
dbSNP: rs121918505
rs121918505
0.851 0.080 10 121520119 missense variant A/G snv
CUI: C0038356
Disease: Stomach Neoplasms
Stomach Neoplasms
0.700 0
dbSNP: rs137854571
rs137854571
APC
1.000 0.120 5 112838793 stop gained C/T snv
CUI: C0038356
Disease: Stomach Neoplasms
Stomach Neoplasms
0.700 0
dbSNP: rs137854573
rs137854573
APC
0.807 0.120 5 112828889 stop gained C/T snv
CUI: C0038356
Disease: Stomach Neoplasms
Stomach Neoplasms
0.700 0
dbSNP: rs137854575
rs137854575
APC
0.807 0.120 5 112838399 stop gained C/A;G;T snv 4.7E-04
CUI: C0038356
Disease: Stomach Neoplasms
Stomach Neoplasms
0.700 0
dbSNP: rs140342925
rs140342925
0.882 0.120 1 45332445 missense variant C/T snv 8.4E-05 8.4E-05
CUI: C0038356
Disease: Stomach Neoplasms
Stomach Neoplasms
0.700 0
dbSNP: rs1434545235
rs1434545235
0.752 0.440 10 121565500 missense variant T/C snv 4.0E-06
CUI: C0038356
Disease: Stomach Neoplasms
Stomach Neoplasms
0.700 0
dbSNP: rs145945630
rs145945630
APC
0.827 0.120 5 112754960 stop gained C/T snv 2.4E-05
CUI: C0038356
Disease: Stomach Neoplasms
Stomach Neoplasms
0.700 0
dbSNP: rs149633775
rs149633775
1.000 0.120 17 7673773 missense variant G/A;C;T snv 7.2E-05; 4.0E-06
CUI: C0038356
Disease: Stomach Neoplasms
Stomach Neoplasms
0.700 0
dbSNP: rs1553125914
rs1553125914
1.000 0.120 1 45331512 frameshift variant -/TC delins
CUI: C0038356
Disease: Stomach Neoplasms
Stomach Neoplasms
0.700 0
dbSNP: rs1554085355
rs1554085355
APC
0.851 0.120 5 112839461 stop gained T/A snv
CUI: C0038356
Disease: Stomach Neoplasms
Stomach Neoplasms
0.700 0
dbSNP: rs1554927408
rs1554927408
0.742 0.480 10 121515254 missense variant C/T snv
CUI: C0038356
Disease: Stomach Neoplasms
Stomach Neoplasms
0.700 0