rs16976358, LINC00907

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.
Child Development Disorders, Pervasive
CUI: C0008074
Disease: Child Development Disorders, Pervasive
379 0.827 0.080 18 42611606 intron variant T/C snv 1.0E-02 0.700 1.000 1 2016 2016
Autism Spectrum Disorders
CUI: C1510586
Disease: Autism Spectrum Disorders
331 0.827 0.080 18 42611606 intron variant T/C snv 1.0E-02 0.010 1.000 1 2017 2017
Autistic Disorder
CUI: C0004352
Disease: Autistic Disorder
395 0.827 0.080 18 42611606 intron variant T/C snv 1.0E-02 0.010 1.000 1 2017 2017
Bipolar Disorder
CUI: C0005586
Disease: Bipolar Disorder
839 0.827 0.080 18 42611606 intron variant T/C snv 1.0E-02 0.010 1.000 1 2017 2017
Essential Tremor
CUI: C0270736
Disease: Essential Tremor
79 0.827 0.080 18 42611606 intron variant T/C snv 1.0E-02 0.010 1.000 1 2017 2017
Parkinson Disease
CUI: C0030567
Disease: Parkinson Disease
990 0.827 0.080 18 42611606 intron variant T/C snv 1.0E-02 0.010 1.000 1 2017 2017