rs7812298, CHRNA6

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.
Dizziness
CUI: C0012833
Disease: Dizziness
14 8 42753436 intron variant C/T snv 0.36 0.010 1.000 1 2014 2014
Vertigo
CUI: C0042571
Disease: Vertigo
35 8 42753436 intron variant C/T snv 0.36 0.010 1.000 1 2014 2014