rs10868235, NTRK2

N. diseases: 6
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.
Epilepsy, Temporal Lobe
CUI: C0014556
Disease: Epilepsy, Temporal Lobe
33 0.925 0.040 9 84878840 intron variant C/T snv 0.40 0.020 1.000 2 2017 2017
Anxiety Disorders
CUI: C0003469
Disease: Anxiety Disorders
163 0.925 0.040 9 84878840 intron variant C/T snv 0.40 0.010 1.000 1 2017 2017
Completed Suicide
CUI: C0852733
Disease: Completed Suicide
33 0.925 0.040 9 84878840 intron variant C/T snv 0.40 0.010 1.000 1 2012 2012
Epilepsy
CUI: C0014544
Disease: Epilepsy
339 0.925 0.040 9 84878840 intron variant C/T snv 0.40 0.010 1.000 1 2017 2017
Mood Disorders
CUI: C0525045
Disease: Mood Disorders
308 0.925 0.040 9 84878840 intron variant C/T snv 0.40 0.010 1.000 1 2017 2017
Psychotic Disorders
CUI: C0033975
Disease: Psychotic Disorders
179 0.925 0.040 9 84878840 intron variant C/T snv 0.40 0.010 1.000 1 2017 2017