Source: CLINVAR

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1555358382
rs1555358382
GCH1
CUI: C0151786
Disease: Muscle Weakness
Muscle Weakness 		A 0.700 GeneticVariation CLINVAR

dbSNP: rs1555358382
rs1555358382
GCH1
CUI: C1836150
Disease: Gait imbalance
Gait imbalance 		A 0.700 GeneticVariation CLINVAR

dbSNP: rs1555358382
rs1555358382
GCH1
CUI: C0575081
Disease: Gait abnormality
Gait abnormality 		A 0.700 GeneticVariation CLINVAR

dbSNP: rs1555358382
rs1555358382
GCH1
CUI: C0751837
Disease: Gait Ataxia
Gait Ataxia 		A 0.700 GeneticVariation CLINVAR

dbSNP: rs1555358382
rs1555358382
GCH1
CUI: C0026837
Disease: Muscle Rigidity
Muscle Rigidity 		A 0.700 GeneticVariation CLINVAR

dbSNP: rs1555358382
rs1555358382
GCH1
CUI: C0037317
Disease: Sleep disturbances
Sleep disturbances 		A 0.700 GeneticVariation CLINVAR