Source: UNIPROT

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: rs121913529
rs121913529
0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma
0.710 1.000 3 1987 2004
dbSNP: rs104894361
rs104894361
0.882 0.240 12 25245370 missense variant T/A;C;G snv 4.0E-06
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma
0.700 1.000 3 1987 2003
dbSNP: rs121908382
rs121908382
1.000 0.080 1 45331530 missense variant G/A snv
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma
0.700 1.000 3 2004 2015
dbSNP: rs121908383
rs121908383
1.000 0.080 1 45331502 missense variant T/C snv
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma
0.700 1.000 3 2004 2015
dbSNP: rs121912469
rs121912469
1.000 0.080 5 132489457 missense variant T/A snv
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma
0.700 1.000 3 1998 2014
dbSNP: rs121913528
rs121913528
0.851 0.160 12 25227349 missense variant C/A;T snv
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma
0.700 1.000 3 1987 2003
dbSNP: rs121913530
rs121913530
0.583 0.640 12 25245351 missense variant C/A;G;T snv
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma
0.700 1.000 3 1987 2003
dbSNP: rs121909776
rs121909776
1.000 0.080 2 201187798 missense variant T/C snv 1.2E-04 2.8E-05
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma
0.700 1.000 2 2002 2014
dbSNP: rs121912470
rs121912470
0.925 0.120 5 132489448 missense variant A/G snv
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma
0.700 1.000 2 1998 1999
dbSNP: rs28933369
rs28933369
0.925 0.080 17 39724744 missense variant G/A snv
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma
0.700 1.000 2 2004 2007
dbSNP: rs28933379
rs28933379
APC
1.000 0.080 5 112838953 missense variant G/A snv
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma
0.700 1.000 1 2014 2014
dbSNP: rs112445441
rs112445441
0.658 0.400 12 25245347 missense variant C/A;G;T snv
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma
0.700 0
dbSNP: rs1203145163
rs1203145163
1.000 0.080 21 42363329 missense variant C/A snv 7.0E-06
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma
0.700 0
dbSNP: rs1400295986
rs1400295986
APC
0.925 0.080 5 112838233 missense variant T/C snv
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma
0.700 0
dbSNP: rs202208566
rs202208566
1.000 0.080 12 109903156 missense variant T/C snv 6.5E-04 1.7E-04
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma
0.700 0
dbSNP: rs367807476
rs367807476
1.000 0.080 19 1223035 missense variant C/G;T snv 9.2E-06 1.4E-05
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma
0.700 0
dbSNP: rs372481703
rs372481703
APC
1.000 0.080 5 112839106 missense variant G/A snv 1.6E-05 1.4E-05
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma
0.700 0