APOE, apolipoprotein E, 348

N. diseases: 1049; N. variants: 62
Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs11542041
rs11542041
0.677 0.480 19 44908690 missense variant C/A;T snv 2.1E-05
CUI: C0020473
Disease: Hyperlipidemia
Hyperlipidemia
Nutritional and Metabolic Diseases 0.010 1.000 1 1988 1988
dbSNP: rs121918392
rs121918392
0.925 0.040 19 44907777 missense variant G/A snv 3.6E-05 7.0E-06
CUI: C0020473
Disease: Hyperlipidemia
Hyperlipidemia
Nutritional and Metabolic Diseases 0.010 1.000 1 2002 2002
dbSNP: rs140808909
rs140808909
0.851 0.120 19 44909080 missense variant G/A snv 2.0E-04 5.6E-05
CUI: C0020473
Disease: Hyperlipidemia
Hyperlipidemia
Nutritional and Metabolic Diseases 0.010 1.000 1 1999 1999
dbSNP: rs267606661
rs267606661
0.763 0.120 19 44909101 missense variant C/G;T snv 3.9E-04; 1.0E-05
CUI: C0020473
Disease: Hyperlipidemia
Hyperlipidemia
Nutritional and Metabolic Diseases 0.010 1.000 1 1997 1997
dbSNP: rs429358
rs429358
0.590 0.600 19 44908684 missense variant T/C snv 0.14 0.16
CUI: C0020473
Disease: Hyperlipidemia
Hyperlipidemia
Nutritional and Metabolic Diseases 0.010 1.000 1 1988 1988
dbSNP: rs573658040
rs573658040
0.790 0.200 19 44908705 missense variant C/G;T snv 6.3E-06
CUI: C0020473
Disease: Hyperlipidemia
Hyperlipidemia
Nutritional and Metabolic Diseases 0.010 1.000 1 1995 1995
dbSNP: rs764929617
rs764929617
0.776 0.200 19 44907799 missense variant C/T snv 4.0E-06
CUI: C0020473
Disease: Hyperlipidemia
Hyperlipidemia
Nutritional and Metabolic Diseases 0.010 1.000 1 2013 2013
dbSNP: rs769455
rs769455
0.827 0.120 19 44908783 missense variant C/T snv 1.4E-03 6.9E-03
CUI: C0020473
Disease: Hyperlipidemia
Hyperlipidemia
Nutritional and Metabolic Diseases 0.010 1.000 1 1995 1995