rs121917893, NLGN3

N. diseases: 10
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.
ASPERGER SYNDROME, X-LINKED, SUSCEPTIBILITY TO, 1 (disorder)
CUI: C1845341
Disease: ASPERGER SYNDROME, X-LINKED, SUSCEPTIBILITY TO, 1 (disorder)
1 0.807 0.160 X 71167508 missense variant C/T snv 0.700 0
AUTISM, X-LINKED, SUSCEPTIBILITY TO, 1 (finding)
CUI: C1845540
Disease: AUTISM, X-LINKED, SUSCEPTIBILITY TO, 1 (finding)
1 0.807 0.160 X 71167508 missense variant C/T snv 0.700 0
Autistic Disorder
CUI: C0004352
Disease: Autistic Disorder
395 0.807 0.160 X 71167508 missense variant C/T snv 0.090 1.000 9 2004 2019
Autism Spectrum Disorders
CUI: C1510586
Disease: Autism Spectrum Disorders
331 0.807 0.160 X 71167508 missense variant C/T snv 0.080 1.000 8 2004 2019
Abnormal behavior
CUI: C0233514
Disease: Abnormal behavior
121 0.807 0.160 X 71167508 missense variant C/T snv 0.010 1.000 1 2018 2018
Congenital Hypothyroidism
CUI: C0010308
Disease: Congenital Hypothyroidism
48 0.807 0.160 X 71167508 missense variant C/T snv 0.010 1.000 1 2010 2010
Gastrointestinal dysfunction
CUI: C0679407
Disease: Gastrointestinal dysfunction
6 0.807 0.160 X 71167508 missense variant C/T snv 0.010 1.000 1 2019 2019
Genitourinary symptoms
CUI: C0426317
Disease: Genitourinary symptoms
1 0.807 0.160 X 71167508 missense variant C/T snv 0.010 1.000 1 2019 2019
Pervasive Development Disorder
CUI: C0524528
Disease: Pervasive Development Disorder
49 0.807 0.160 X 71167508 missense variant C/T snv 0.010 1.000 1 2004 2004
Social Communication Disorder
CUI: C0150080
Disease: Social Communication Disorder
4 0.807 0.160 X 71167508 missense variant C/T snv 0.010 1.000 1 2007 2007