Source: GWASDB

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: rs671
rs671
0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03
CUI: C0014859
Disease: Esophageal Neoplasms
Esophageal Neoplasms
0.880 1.000 1 2001 2019
dbSNP: rs1229984
rs1229984
0.570 0.560 4 99318162 missense variant T/C;G snv 0.90
CUI: C0014859
Disease: Esophageal Neoplasms
Esophageal Neoplasms
0.840 1.000 1 2009 2016
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: rs738722
rs738722
0.882 0.120 22 28734024 intron variant T/C snv 0.67
CUI: C0014859
Disease: Esophageal Neoplasms
Esophageal Neoplasms
0.810 1.000 1 2010 2012
dbSNP: rs1042026
rs1042026
1.000 0.080 4 99307309 3 prime UTR variant T/C snv 0.24
CUI: C0014859
Disease: Esophageal Neoplasms
Esophageal Neoplasms
0.800 1.000 2 2010 2012
dbSNP: rs3805322
rs3805322
1.000 0.080 4 99135847 intron variant A/G snv 1.1E-02
CUI: C0014859
Disease: Esophageal Neoplasms
Esophageal Neoplasms
0.800 1.000 2 2010 2012
dbSNP: rs11066280
rs11066280
0.742 0.280 12 112379979 intron variant T/A snv 7.0E-03
CUI: C0014859
Disease: Esophageal Neoplasms
Esophageal Neoplasms
0.800 1.000 1 2010 2011
dbSNP: rs17450420
rs17450420
13 104386796 intergenic variant A/G snv 5.9E-02
CUI: C0014859
Disease: Esophageal Neoplasms
Esophageal Neoplasms
0.800 1.000 1 2012 2012
dbSNP: rs17761864
rs17761864
1.000 0.040 17 2268343 intron variant C/A snv 0.28
CUI: C0014859
Disease: Esophageal Neoplasms
Esophageal Neoplasms
0.800 1.000 1 2012 2012
dbSNP: rs2074356
rs2074356
0.763 0.280 12 112207597 intron variant G/A snv 3.8E-03
CUI: C0014859
Disease: Esophageal Neoplasms
Esophageal Neoplasms
0.800 1.000 1 2010 2011
dbSNP: rs2239612
rs2239612
1.000 0.040 3 187075454 intron variant G/A snv 0.17
CUI: C0014859
Disease: Esophageal Neoplasms
Esophageal Neoplasms
0.800 1.000 1 2012 2012
dbSNP: rs2239815
rs2239815
0.925 0.080 22 28796682 non coding transcript exon variant T/C snv 0.44
CUI: C0014859
Disease: Esophageal Neoplasms
Esophageal Neoplasms
0.800 1.000 1 2012 2012
dbSNP: rs2847281
rs2847281
1.000 0.040 18 12821594 intron variant A/G snv 0.32
CUI: C0014859
Disease: Esophageal Neoplasms
Esophageal Neoplasms
0.800 1.000 1 2012 2012
dbSNP: rs4785204
rs4785204
1.000 0.040 16 50069823 intron variant C/T snv 8.6E-02
CUI: C0014859
Disease: Esophageal Neoplasms
Esophageal Neoplasms
0.800 1.000 1 2012 2012
dbSNP: rs4822983
rs4822983
0.925 0.080 22 28719078 intron variant C/T snv 0.33
CUI: C0014859
Disease: Esophageal Neoplasms
Esophageal Neoplasms
0.800 1.000 1 2012 2012
dbSNP: rs6503659
rs6503659
1.000 0.040 17 41741012 intergenic variant A/C;G;T snv
CUI: C0014859
Disease: Esophageal Neoplasms
Esophageal Neoplasms
0.800 1.000 1 2012 2012
dbSNP: rs9288520
rs9288520
2 216616548 intergenic variant G/A snv 0.14
CUI: C0014859
Disease: Esophageal Neoplasms
Esophageal Neoplasms
0.800 1.000 1 2012 2012
dbSNP: rs13042395
rs13042395
0.752 0.160 20 773867 intron variant C/T snv 5.9E-02
CUI: C0014859
Disease: Esophageal Neoplasms
Esophageal Neoplasms
0.730 0.750 1 2010 2016
dbSNP: rs10931936
rs10931936
0.827 0.120 2 201279205 intron variant T/C snv 0.72
CUI: C0014859
Disease: Esophageal Neoplasms
Esophageal Neoplasms
0.710 1.000 1 2012 2017
dbSNP: rs13016963
rs13016963
0.851 0.080 2 201298088 intron variant A/G snv 0.59
CUI: C0014859
Disease: Esophageal Neoplasms
Esophageal Neoplasms
0.710 1.000 1 2012 2017
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: rs1000668
rs1000668
9 72790943 intron variant T/A;G snv
CUI: C0014859
Disease: Esophageal Neoplasms
Esophageal Neoplasms
0.700 1.000 1 2012 2012
dbSNP: rs10186527
rs10186527
2 201335852 intron variant C/T snv 0.54
CUI: C0014859
Disease: Esophageal Neoplasms
Esophageal Neoplasms
0.700 1.000 1 2012 2012