rs11466112, NGF-AS1;NGF

N. diseases: 3
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 115286135 missense variant G/A snv 1.6E-05 7.0E-06 0.710 1.000 1 2019 2019
Pain
CUI: C0030193
Disease: Pain
196 1.000 0.080 1 115286135 missense variant G/A snv 1.6E-05 7.0E-06 0.030 1.000 3 2009 2019
Deep pain
CUI: C0234229
Disease: Deep pain
1 1.000 0.080 1 115286135 missense variant G/A snv 1.6E-05 7.0E-06 0.010 1.000 1 2009 2009