rs2710102, CNTNAP2

N. diseases: 12
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 0.790 0.120 7 147877298 intron variant A/G;T snv 0.700 0
Autism Spectrum Disorders
CUI: C1510586
Disease: Autism Spectrum Disorders
331 0.790 0.120 7 147877298 intron variant A/G;T snv 0.030 1.000 3 2011 2019
Autistic Disorder
CUI: C0004352
Disease: Autistic Disorder
395 0.790 0.120 7 147877298 intron variant A/G;T snv 0.020 0.500 2 2011 2013
Abnormal behavior
CUI: C0233514
Disease: Abnormal behavior
121 0.790 0.120 7 147877298 intron variant A/G;T snv 0.010 1 2018 2018
Language Disorders
CUI: C0023015
Disease: Language Disorders
25 0.790 0.120 7 147877298 intron variant A/G;T snv 0.010 1.000 1 2011 2011
Major Depressive Disorder
CUI: C1269683
Disease: Major Depressive Disorder
1451 0.790 0.120 7 147877298 intron variant A/G;T snv 0.010 1.000 1 2013 2013
Mental disorders
CUI: C0004936
Disease: Mental disorders
149 0.790 0.120 7 147877298 intron variant A/G;T snv 0.010 1 2018 2018
Schizophrenia
CUI: C0036341
Disease: Schizophrenia
2897 0.790 0.120 7 147877298 intron variant A/G;T snv 0.010 1.000 1 2013 2013
Selective Mutism
CUI: C0236818
Disease: Selective Mutism
2 0.790 0.120 7 147877298 intron variant A/G;T snv 0.010 1.000 1 2011 2011
Selective mutism specific to childhood and adolescence
2 0.790 0.120 7 147877298 intron variant A/G;T snv 0.010 1.000 1 2011 2011
Specific language impairment
CUI: C0454651
Disease: Specific language impairment
9 0.790 0.120 7 147877298 intron variant A/G;T snv 0.010 1.000 1 2011 2011
Unipolar Depression
CUI: C0041696
Disease: Unipolar Depression
225 0.790 0.120 7 147877298 intron variant A/G;T snv 0.010 1.000 1 2013 2013