Source: ALL

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: rs1143684
rs1143684
0.882 0.160 6 3010156 missense variant C/T snv 0.79 0.84
CUI: C0235974
Disease: Pancreatic carcinoma
Pancreatic carcinoma
0.010 1.000 1 2011 2011
dbSNP: rs1143684
rs1143684
0.882 0.160 6 3010156 missense variant C/T snv 0.79 0.84
CUI: C0346647
Disease: Malignant neoplasm of pancreas
Malignant neoplasm of pancreas
0.010 1.000 1 2011 2011
dbSNP: rs1143684
rs1143684
0.882 0.160 6 3010156 missense variant C/T snv 0.79 0.84
CUI: C0338656
Disease: Impaired cognition
Impaired cognition
0.010 1.000 1 2010 2010
dbSNP: rs1143684
rs1143684
0.882 0.160 6 3010156 missense variant C/T snv 0.79 0.84
CUI: C0234985
Disease: Mental deterioration
Mental deterioration
0.010 1.000 1 2010 2010