rs77485247, HRH4

N. diseases: 3
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.
Aortic Valve Insufficiency
CUI: C0003504
Disease: Aortic Valve Insufficiency
8 0.925 0.080 18 24460578 upstream gene variant T/A snv 0.010 1.000 1 2017 2017
Meniere Disease
CUI: C0025281
Disease: Meniere Disease
36 0.925 0.080 18 24460578 upstream gene variant T/A snv 0.010 1.000 1 2019 2019
Vertigo
CUI: C0042571
Disease: Vertigo
35 0.925 0.080 18 24460578 upstream gene variant T/A snv 0.010 1.000 1 2019 2019