rs7794745, CNTNAP2

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.
AUTISM, SUSCEPTIBILITY TO, 15
CUI: C2677504
Disease: AUTISM, SUSCEPTIBILITY TO, 15
3 0.851 0.040 7 146792514 intron variant A/T snv 0.49 0.700 0
Autism Spectrum Disorders
CUI: C1510586
Disease: Autism Spectrum Disorders
331 0.851 0.040 7 146792514 intron variant A/T snv 0.49 0.040 1.000 4 2010 2019
Autistic Disorder
CUI: C0004352
Disease: Autistic Disorder
395 0.851 0.040 7 146792514 intron variant A/T snv 0.49 0.040 0.750 4 2011 2017
Attention deficit hyperactivity disorder
420 0.851 0.040 7 146792514 intron variant A/T snv 0.49 0.010 1.000 1 2010 2010
Language Disorders
CUI: C0023015
Disease: Language Disorders
25 0.851 0.040 7 146792514 intron variant A/T snv 0.49 0.010 1.000 1 2011 2011
Substance Use Disorders
CUI: C0038586
Disease: Substance Use Disorders
16 0.851 0.040 7 146792514 intron variant A/T snv 0.49 0.010 1.000 1 2010 2010