TPH2, tryptophan hydroxylase 2, 121278

N. diseases: 137; N. variants: 37
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: rs139896303
rs139896303
1.000 0.040 12 71972584 missense variant G/A snv 1.2E-04 5.6E-05
CUI: C1510586
Disease: Autism Spectrum Disorders
Autism Spectrum Disorders
Mental Disorders 0.010 1.000 1 2012 2012
dbSNP: rs1843809
rs1843809
0.851 0.080 12 71954918 intron variant G/T snv 0.77
CUI: C1510586
Disease: Autism Spectrum Disorders
Autism Spectrum Disorders
Mental Disorders 0.010 1.000 1 2010 2010
dbSNP: rs2129575
rs2129575
1.000 0.040 12 71946293 intron variant G/T snv 0.25
CUI: C1510586
Disease: Autism Spectrum Disorders
Autism Spectrum Disorders
Mental Disorders 0.010 1.000 1 2012 2012