rs3840634, CAV1

N. diseases: 2
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.
Meniere Disease
CUI: C0025281
Disease: Meniere Disease
36 0.925 0.120 7 116556798 intron variant T/C snv 0.010 1.000 1 2013 2013
Sudden sensorineural hearing loss
CUI: C4275242
Disease: Sudden sensorineural hearing loss
38 0.925 0.120 7 116556798 intron variant T/C snv 0.010 1.000 1 2013 2013