rs1566658823, GCH1

N. diseases: 4
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.
Coughing
CUI: C0010200
Disease: Coughing
16 1.000 0.120 14 54844138 missense variant A/G snv 0.700 0
Dystonia
CUI: C0013421
Disease: Dystonia
97 1.000 0.120 14 54844138 missense variant A/G snv 0.700 0
Hyperphenylalaninemia, BH4-Deficient, B
CUI: C0268467
Disease: Hyperphenylalaninemia, BH4-Deficient, B
13 1.000 0.120 14 54844138 missense variant A/G snv 0.700 0
Poor eye contact
CUI: C1445953
Disease: Poor eye contact
6 1.000 0.120 14 54844138 missense variant A/G snv 0.700 0