rs1783901, SCN3B

N. diseases: 1
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.
Vertigo
CUI: C0042571
Disease: Vertigo
35 11 123642798 intron variant C/T snv 0.24 0.010 1.000 1 2018 2018