Source: ALL

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: rs12610531
rs12610531
0.925 0.080 19 5559819 3 prime UTR variant G/A;C snv
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma
0.010 1.000 1 2016 2016
dbSNP: rs12610531
rs12610531
0.925 0.080 19 5559819 3 prime UTR variant G/A;C snv
CUI: C0024623
Disease: Malignant neoplasm of stomach
Malignant neoplasm of stomach
0.010 1.000 1 2016 2016
dbSNP: rs2288947
rs2288947
0.827 0.160 19 5562104 3 prime UTR variant G/A snv 0.45
CUI: C0024623
Disease: Malignant neoplasm of stomach
Malignant neoplasm of stomach
0.010 1.000 1 2016 2016
dbSNP: rs2288947
rs2288947
0.827 0.160 19 5562104 3 prime UTR variant G/A snv 0.45
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.010 1.000 1 2017 2017
dbSNP: rs2288947
rs2288947
0.827 0.160 19 5562104 3 prime UTR variant G/A snv 0.45
Secondary malignant neoplasm of lymph node
0.010 1.000 1 2017 2017
dbSNP: rs2288947
rs2288947
0.827 0.160 19 5562104 3 prime UTR variant G/A snv 0.45
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma
0.010 1.000 1 2016 2016
dbSNP: rs2288947
rs2288947
0.827 0.160 19 5562104 3 prime UTR variant G/A snv 0.45
CUI: C4552766
Disease: Miscarriage
Miscarriage
0.010 < 0.001 1 2019 2019
dbSNP: rs8105637
rs8105637
0.925 0.120 19 5566221 intron variant A/G snv 0.56
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.010 1.000 1 2017 2017
dbSNP: rs8105637
rs8105637
0.925 0.120 19 5566221 intron variant A/G snv 0.56
Secondary malignant neoplasm of lymph node
0.010 1.000 1 2017 2017
dbSNP: rs8113645
rs8113645
0.925 0.080 19 5561065 3 prime UTR variant A/G;T snv
CUI: C0024623
Disease: Malignant neoplasm of stomach
Malignant neoplasm of stomach
0.010 1.000 1 2016 2016
dbSNP: rs8113645
rs8113645
0.925 0.080 19 5561065 3 prime UTR variant A/G;T snv
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma
0.010 1.000 1 2016 2016