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: rs2274223
rs2274223
0.620 0.400 10 94306584 missense variant A/G snv 0.28 0.31
CUI: C0014859
Disease: Esophageal Neoplasms
Esophageal Neoplasms
0.900 0.938 2 2010 2019
dbSNP: rs3765524
rs3765524
0.724 0.320 10 94298541 missense variant C/T snv 0.27 0.31
CUI: C0014859
Disease: Esophageal Neoplasms
Esophageal Neoplasms
0.820 1.000 2 2010 2019
dbSNP: rs12263737
rs12263737
1.000 0.080 10 94285156 intron variant G/A snv 0.32
CUI: C0014859
Disease: Esophageal Neoplasms
Esophageal Neoplasms
0.700 1.000 2 2010 2012
dbSNP: rs3781264
rs3781264
0.851 0.120 10 94310618 intron variant A/G snv 0.25
CUI: C0014859
Disease: Esophageal Neoplasms
Esophageal Neoplasms
0.700 1.000 2 2010 2012
dbSNP: rs11187842
rs11187842
0.925 0.080 10 94292754 intron variant C/T snv 7.8E-02
CUI: C0014859
Disease: Esophageal Neoplasms
Esophageal Neoplasms
0.700 1.000 1 2012 2012
dbSNP: rs3740360
rs3740360
0.827 0.240 10 94265734 intron variant A/C snv 9.7E-02 8.4E-02
CUI: C0014859
Disease: Esophageal Neoplasms
Esophageal Neoplasms
0.700 1.000 1 2012 2012
dbSNP: rs753724
rs753724
0.882 0.080 10 94291660 intron variant G/A;C;T snv
CUI: C0014859
Disease: Esophageal Neoplasms
Esophageal Neoplasms
0.700 1.000 1 2012 2012