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: rs13016963
rs13016963
0.851 0.080 2 201298088 intron variant A/G snv 0.59
CUI: C0025202
Disease: melanoma
melanoma
0.800 1.000 1 2011 2017
dbSNP: rs6715284
rs6715284
1.000 0.120 2 201289674 intron variant C/G;T snv 0.12
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis
0.800 1.000 1 2014 2019
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: 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
dbSNP: rs10197246
rs10197246
2 201340018 intron variant T/C snv 0.72
CUI: C0014859
Disease: Esophageal Neoplasms
Esophageal Neoplasms
0.700 1.000 1 2012 2012
dbSNP: rs10201587
rs10201587
2 201338068 intron variant A/G snv 0.47
CUI: C0014859
Disease: Esophageal Neoplasms
Esophageal Neoplasms
0.700 1.000 1 2012 2012
dbSNP: rs1035142
rs1035142
0.807 0.200 2 201288355 3 prime UTR variant T/C;G snv 0.54
CUI: C0025202
Disease: melanoma
melanoma
0.700 1.000 1 2011 2011
dbSNP: rs10454127
rs10454127
2 201347651 intron variant G/A;T snv
CUI: C0014859
Disease: Esophageal Neoplasms
Esophageal Neoplasms
0.700 1.000 1 2012 2012
dbSNP: rs11898821
rs11898821
2 201334965 intron variant T/C snv 0.46
CUI: C0014859
Disease: Esophageal Neoplasms
Esophageal Neoplasms
0.700 1.000 1 2012 2012
dbSNP: rs2080304
rs2080304
2 201321699 intron variant G/C snv 0.59
CUI: C0014859
Disease: Esophageal Neoplasms
Esophageal Neoplasms
0.700 1.000 1 2012 2012
dbSNP: rs2110690
rs2110690
2 201320409 intron variant A/G snv 0.42
CUI: C0014859
Disease: Esophageal Neoplasms
Esophageal Neoplasms
0.700 1.000 1 2012 2012
dbSNP: rs2349073
rs2349073
2 201322263 intron variant C/A snv 0.75
CUI: C0014859
Disease: Esophageal Neoplasms
Esophageal Neoplasms
0.700 1.000 1 2012 2012
dbSNP: rs6435079
rs6435079
2 201335608 intron variant C/G;T snv
CUI: C0014859
Disease: Esophageal Neoplasms
Esophageal Neoplasms
0.700 1.000 1 2012 2012
dbSNP: rs6714736
rs6714736
2 201349425 intron variant C/T snv 0.63
CUI: C0014859
Disease: Esophageal Neoplasms
Esophageal Neoplasms
0.700 1.000 1 2012 2012
dbSNP: rs6719014
rs6719014
2 201311301 intron variant T/C snv 0.72
CUI: C0014859
Disease: Esophageal Neoplasms
Esophageal Neoplasms
0.700 1.000 1 2012 2012
dbSNP: rs6731171
rs6731171
2 201314288 intron variant T/A snv 0.59
CUI: C0014859
Disease: Esophageal Neoplasms
Esophageal Neoplasms
0.700 1.000 1 2012 2012
dbSNP: rs6735641
rs6735641
2 201315768 intron variant T/C snv 0.54
CUI: C0014859
Disease: Esophageal Neoplasms
Esophageal Neoplasms
0.700 1.000 1 2012 2012
dbSNP: rs6745435
rs6745435
2 201337840 intron variant G/A snv 0.47
CUI: C0014859
Disease: Esophageal Neoplasms
Esophageal Neoplasms
0.700 1.000 1 2012 2012
dbSNP: rs6757783
rs6757783
2 201335101 intron variant C/T snv 0.63
CUI: C0014859
Disease: Esophageal Neoplasms
Esophageal Neoplasms
0.700 1.000 1 2012 2012
dbSNP: rs700635
rs700635
0.925 0.040 2 201288502 3 prime UTR variant C/A snv 0.72
CUI: C0025202
Disease: melanoma
melanoma
0.700 1.000 1 2011 2011
dbSNP: rs7579792
rs7579792
2 201335727 intron variant A/G snv 0.86
CUI: C0014859
Disease: Esophageal Neoplasms
Esophageal Neoplasms
0.700 1.000 1 2012 2012
dbSNP: rs7582362
rs7582362
2 201311571 intron variant A/G snv 0.72
CUI: C0014859
Disease: Esophageal Neoplasms
Esophageal Neoplasms
0.700 1.000 1 2012 2012
dbSNP: rs7597617
rs7597617
2 201338512 intron variant G/A snv 0.63
CUI: C0014859
Disease: Esophageal Neoplasms
Esophageal Neoplasms
0.700 1.000 1 2012 2012
dbSNP: rs9288318
rs9288318
2 201331340 intron variant C/A snv 0.63
CUI: C0014859
Disease: Esophageal Neoplasms
Esophageal Neoplasms
0.700 1.000 1 2012 2012