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: rs2275913
rs2275913
0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma
0.100 0.857 14 2012 2018
dbSNP: rs397507444
rs397507444
0.405 0.880 1 11794407 missense variant T/G snv
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma
0.100 0.833 12 2005 2014
dbSNP: rs751402
rs751402
0.724 0.360 13 102845848 5 prime UTR variant A/G snv 0.76
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma
0.100 0.833 12 2012 2019
dbSNP: rs13361707
rs13361707
0.882 0.120 5 40791782 intron variant C/T snv 0.31
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma
0.780 1.000 11 2011 2018
dbSNP: rs1131691014
rs1131691014
0.439 0.800 17 7676154 frameshift variant -/C ins
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma
0.080 0.875 8 2009 2015
dbSNP: rs3748067
rs3748067
0.672 0.320 6 52190541 3 prime UTR variant C/T snv 6.2E-02
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma
0.080 0.750 8 2012 2018
dbSNP: rs878854066
rs878854066
0.439 0.800 17 7676153 missense variant GG/AC mnv
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma
0.080 0.875 8 2009 2015
dbSNP: rs1805192
rs1805192
0.510 0.840 3 12379739 missense variant C/G snv
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma
0.070 1.000 7 2008 2015
dbSNP: rs2094258
rs2094258
0.701 0.280 13 102844409 intron variant C/T snv 0.18
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma
0.060 0.833 6 2016 2019
dbSNP: rs10505477
rs10505477
0.658 0.400 8 127395198 intron variant A/G snv 0.40
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma
0.040 1.000 4 2014 2016
dbSNP: rs13042395
rs13042395
0.752 0.160 20 773867 intron variant C/T snv 5.9E-02
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma
0.040 0.750 4 2011 2017
dbSNP: rs1800796
rs1800796
0.555 0.760 7 22726627 non coding transcript exon variant G/C snv 9.9E-02
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma
0.040 1.000 4 2012 2019
dbSNP: rs1800871
rs1800871
0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma
0.040 1.000 4 2011 2019
dbSNP: rs4073
rs4073
0.566 0.800 4 73740307 upstream gene variant A/T snv 0.46
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma
0.040 1.000 4 2012 2018
dbSNP: rs4938723
rs4938723
0.574 0.680 11 111511840 intron variant T/C snv 0.32
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma
0.040 0.750 4 2014 2019
dbSNP: rs920778
rs920778
0.633 0.480 12 53966448 intron variant G/A snv 0.57
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma
0.040 1.000 4 2015 2020
dbSNP: rs10074991
rs10074991
0.851 0.120 5 40790449 intron variant G/A snv 0.31
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma
0.720 1.000 3 2014 2018
dbSNP: rs10889677
rs10889677
0.627 0.720 1 67259437 3 prime UTR variant C/A snv 0.27
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma
0.030 1.000 3 2011 2019
dbSNP: rs11536889
rs11536889
0.658 0.560 9 117715853 3 prime UTR variant G/C snv 0.11
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma
0.030 1.000 3 2011 2014
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: rs13420827
rs13420827
0.882 0.160 2 25231099 3 prime UTR variant C/G;T snv
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma
0.030 1.000 3 2012 2018