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: rs4788074
rs4788074
16 28582276 intron variant G/A snv 0.32
CUI: C0014859
Disease: Esophageal Neoplasms
Esophageal Neoplasms
0.700 1.000 1 2012 2012
dbSNP: rs9924471
rs9924471
1.000 0.120 16 28580209 intron variant G/A snv 0.16
Diabetes Mellitus, Insulin-Dependent
0.700 1.000 1 2011 2011