rs3816873, MTTP

N. diseases: 9
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.
Dyslipidemias
CUI: C0242339
Disease: Dyslipidemias
184 0.790 0.200 4 99583507 missense variant T/C snv 0.25 0.26 0.010 1.000 1 2006 2006
Fatty Liver, Alcoholic
CUI: C0015696
Disease: Fatty Liver, Alcoholic
6 0.790 0.200 4 99583507 missense variant T/C snv 0.25 0.26 0.010 1.000 1 2009 2009
Hyperlipidemia
CUI: C0020473
Disease: Hyperlipidemia
83 0.790 0.200 4 99583507 missense variant T/C snv 0.25 0.26 0.010 1.000 1 2015 2015
Hypobetalipoproteinemias
CUI: C0020597
Disease: Hypobetalipoproteinemias
11 0.790 0.200 4 99583507 missense variant T/C snv 0.25 0.26 0.010 1.000 1 2004 2004
Impaired glucose tolerance
CUI: C0271650
Disease: Impaired glucose tolerance
81 0.790 0.200 4 99583507 missense variant T/C snv 0.25 0.26 0.010 1.000 1 2006 2006
Insulin resistance syndrome
CUI: C3714619
Disease: Insulin resistance syndrome
15 0.790 0.200 4 99583507 missense variant T/C snv 0.25 0.26 0.010 1.000 1 2006 2006
Metabolic Syndrome X
CUI: C0524620
Disease: Metabolic Syndrome X
591 0.790 0.200 4 99583507 missense variant T/C snv 0.25 0.26 0.010 1.000 1 2006 2006
Non-alcoholic Fatty Liver Disease
CUI: C0400966
Disease: Non-alcoholic Fatty Liver Disease
222 0.790 0.200 4 99583507 missense variant T/C snv 0.25 0.26 0.010 1.000 1 2011 2011
Obesity
CUI: C0028754
Disease: Obesity
1111 0.790 0.200 4 99583507 missense variant T/C snv 0.25 0.26 0.010 1.000 1 2009 2009