rs1805055, HTR2A

N. diseases: 3
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.
Neuroleptic Malignant Syndrome
CUI: C0027849
Disease: Neuroleptic Malignant Syndrome
4 0.882 0.120 13 46895833 missense variant G/C;T snv 2.0E-05; 1.8E-02 0.010 1.000 1 1998 1998
Schizophrenia
CUI: C0036341
Disease: Schizophrenia
2897 0.882 0.120 13 46895833 missense variant G/C;T snv 2.0E-05; 1.8E-02 0.010 1.000 1 1997 1997
Taq1A POLYMORPHISM
CUI: C4694057
Disease: Taq1A POLYMORPHISM
14 0.882 0.120 13 46895833 missense variant G/C;T snv 2.0E-05; 1.8E-02 0.010 1.000 1 2007 2007