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: rs3769825
rs3769825
0.925 0.120 2 201246657 intron variant A/G snv 0.46
CUI: C0023434
Disease: Chronic Lymphocytic Leukemia
Chronic Lymphocytic Leukemia
0.800 1.000 1 2013 2013
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: rs10931936
rs10931936
0.827 0.120 2 201279205 intron variant T/C snv 0.72
CUI: C0025202
Disease: melanoma
melanoma
0.700 1.000 1 2011 2011