NLGN3, neuroligin 3, 54413

N. diseases: 63; N. variants: 7
Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs121917893
rs121917893
0.807 0.160 X 71167508 missense variant C/T snv
CUI: C1510586
Disease: Autism Spectrum Disorders
Autism Spectrum Disorders
Mental Disorders 0.080 1.000 8 2004 2019
dbSNP: rs11795613
rs11795613
0.925 0.120 X 71147478 intron variant A/G snv
CUI: C1510586
Disease: Autism Spectrum Disorders
Autism Spectrum Disorders
Mental Disorders 0.010 1.000 1 2011 2011
dbSNP: rs4844285
rs4844285
0.925 0.120 X 71150394 intron variant G/A snv
CUI: C1510586
Disease: Autism Spectrum Disorders
Autism Spectrum Disorders
Mental Disorders 0.010 1.000 1 2011 2011
dbSNP: rs4844286
rs4844286
1.000 0.040 X 71151724 intron variant T/G snv
CUI: C1510586
Disease: Autism Spectrum Disorders
Autism Spectrum Disorders
Mental Disorders 0.010 1.000 1 2011 2011
dbSNP: rs878853147
rs878853147
0.925 0.200 X 71169399 missense variant C/T snv
CUI: C1510586
Disease: Autism Spectrum Disorders
Autism Spectrum Disorders
Mental Disorders 0.010 1.000 1 2019 2019