rs4668123, LRP2

N. diseases: 6
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Acute Chest Syndrome
CUI: C0742343
Disease: Acute Chest Syndrome
135 0.851 0.280 2 169196995 missense variant C/A;G;T snv 0.010 1.000 1 2020 2020
Acute Coronary Syndrome
CUI: C0948089
Disease: Acute Coronary Syndrome
139 0.851 0.280 2 169196995 missense variant C/A;G;T snv 0.010 1.000 1 2020 2020
Cognitive changes
CUI: C1392786
Disease: Cognitive changes
15 0.851 0.280 2 169196995 missense variant C/A;G;T snv 0.010 1.000 1 2012 2012
hearing impairment
CUI: C1384666
Disease: hearing impairment
337 0.851 0.280 2 169196995 missense variant C/A;G;T snv 0.010 1.000 1 2008 2008
Malignant neoplasm of pancreas
CUI: C0346647
Disease: Malignant neoplasm of pancreas
277 0.851 0.280 2 169196995 missense variant C/A;G;T snv 0.010 1.000 1 2015 2015
Pancreatic carcinoma
CUI: C0235974
Disease: Pancreatic carcinoma
322 0.851 0.280 2 169196995 missense variant C/A;G;T snv 0.010 1.000 1 2015 2015