rs11709492, SCN11A

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.
Pain
CUI: C0030193
Disease: Pain
196 3 38904493 intron variant C/T snv 0.26 0.010 1.000 1 2017 2017