Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs2274223
rs2274223
0.620 0.400 10 94306584 missense variant A/G snv 0.28 0.31
CUI: C0546837
Disease: Malignant neoplasm of esophagus
Malignant neoplasm of esophagus
Digestive System Diseases; Neoplasms 0.800 0.929 14 2011 2019
dbSNP: rs10882424
rs10882424
1.000 0.080 10 94326321 intron variant T/G snv 0.31
CUI: C0546837
Disease: Malignant neoplasm of esophagus
Malignant neoplasm of esophagus
Digestive System Diseases; Neoplasms 0.700 1.000 1 2011 2011
dbSNP: rs10882430
rs10882430
1.000 0.080 10 94330915 3 prime UTR variant A/G snv 0.31
CUI: C0546837
Disease: Malignant neoplasm of esophagus
Malignant neoplasm of esophagus
Digestive System Diseases; Neoplasms 0.700 1.000 1 2011 2011
dbSNP: rs11187844
rs11187844
1.000 0.080 10 94296872 intron variant C/A snv 0.12
CUI: C0546837
Disease: Malignant neoplasm of esophagus
Malignant neoplasm of esophagus
Digestive System Diseases; Neoplasms 0.700 1.000 1 2011 2011
dbSNP: rs11187853
rs11187853
1.000 0.080 10 94312471 intron variant G/A;C snv
CUI: C0546837
Disease: Malignant neoplasm of esophagus
Malignant neoplasm of esophagus
Digestive System Diseases; Neoplasms 0.700 1.000 1 2011 2011
dbSNP: rs11187876
rs11187876
1.000 0.080 10 94330382 3 prime UTR variant C/T snv 0.31
CUI: C0546837
Disease: Malignant neoplasm of esophagus
Malignant neoplasm of esophagus
Digestive System Diseases; Neoplasms 0.700 1.000 1 2011 2011
dbSNP: rs6583937
rs6583937
1.000 0.080 10 94323695 intron variant A/G snv 0.32
CUI: C0546837
Disease: Malignant neoplasm of esophagus
Malignant neoplasm of esophagus
Digestive System Diseases; Neoplasms 0.700 1.000 1 2011 2011
dbSNP: rs3765524
rs3765524
0.724 0.320 10 94298541 missense variant C/T snv 0.27 0.31
CUI: C0546837
Disease: Malignant neoplasm of esophagus
Malignant neoplasm of esophagus
Digestive System Diseases; Neoplasms 0.020 1.000 2 2014 2019
dbSNP: rs10509670
rs10509670
0.851 0.080 10 94308190 intron variant A/G snv 0.30
CUI: C0546837
Disease: Malignant neoplasm of esophagus
Malignant neoplasm of esophagus
Digestive System Diseases; Neoplasms 0.010 1.000 1 2019 2019
dbSNP: rs2274224
rs2274224
0.882 0.080 10 94279840 missense variant G/A;C snv 8.8E-05; 0.44
CUI: C0546837
Disease: Malignant neoplasm of esophagus
Malignant neoplasm of esophagus
Digestive System Diseases; Neoplasms 0.010 1.000 1 2013 2013
dbSNP: rs776933870
rs776933870
0.925 0.080 10 94306632 missense variant A/G snv 8.0E-06
CUI: C0546837
Disease: Malignant neoplasm of esophagus
Malignant neoplasm of esophagus
Digestive System Diseases; Neoplasms 0.010 1.000 1 2014 2014
dbSNP: rs7922612
rs7922612
0.752 0.080 10 94051682 intron variant C/T snv 0.39
CUI: C0546837
Disease: Malignant neoplasm of esophagus
Malignant neoplasm of esophagus
Digestive System Diseases; Neoplasms 0.010 1.000 1 2014 2014