rs778056858, NTRK1

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.
Hereditary Sensory Autonomic Neuropathy, Type 5
5 1.000 0.080 1 156866944 missense variant T/C snv 8.0E-06 7.0E-06 0.030 1.000 3 2010 2018
Pain
CUI: C0030193
Disease: Pain
196 1.000 0.080 1 156866944 missense variant T/C snv 8.0E-06 7.0E-06 0.020 1.000 2 2010 2011