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: rs7305115
rs7305115
0.807 0.200 12 71979082 synonymous variant A/C;G;T snv 4.0E-06; 0.56
CUI: C0011581
Disease: Depressive disorder
Depressive disorder
Mental Disorders 0.020 1.000 2 2014 2015
dbSNP: rs120074175
rs120074175
0.827 0.080 12 72031544 missense variant G/A snv 1.2E-05 7.0E-06
CUI: C0011581
Disease: Depressive disorder
Depressive disorder
Mental Disorders 0.010 1.000 1 2013 2013
dbSNP: rs12229394
rs12229394
0.925 0.080 12 71999134 intron variant G/A snv 0.29
CUI: C0011581
Disease: Depressive disorder
Depressive disorder
Mental Disorders 0.010 1.000 1 2010 2010
dbSNP: rs78162420
rs78162420
0.882 0.120 12 71941600 missense variant C/A snv 2.1E-03 7.1E-04
CUI: C0011581
Disease: Depressive disorder
Depressive disorder
Mental Disorders 0.010 1.000 1 2017 2017