rs2281997, ENHO

N. diseases: 5
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.
Atherogenic dyslipidaemia
CUI: C4524040
Disease: Atherogenic dyslipidaemia
9 0.882 0.240 9 34521869 intron variant T/A;C snv 0.010 1.000 1 2018 2018
Dyslipidemias
CUI: C0242339
Disease: Dyslipidemias
184 0.882 0.240 9 34521869 intron variant T/A;C snv 0.010 1.000 1 2018 2018
Hodgkin Disease
CUI: C0019829
Disease: Hodgkin Disease
148 0.882 0.240 9 34521869 intron variant T/A;C snv 0.010 1.000 1 2018 2018
Huntington Disease
CUI: C0020179
Disease: Huntington Disease
115 0.882 0.240 9 34521869 intron variant T/A;C snv 0.010 1.000 1 2018 2018
Hyperactive behavior
CUI: C0424295
Disease: Hyperactive behavior
112 0.882 0.240 9 34521869 intron variant T/A;C snv 0.010 1.000 1 2018 2018