FHL1, four and a half LIM domains 1, 2273

N. diseases: 195; N. variants: 22
Disease: REDUCING BODY MYOPATHY, X-LINKED 1A, SEVERE, WITH INFANTILE OR EARLY CHILDHOOD ONSET ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs122458142
rs122458142
Entrez Id: 2273
Gene Symbol: FHL1
FHL1
CUI: C4225423
Disease:
REDUCING BODY MYOPATHY, X-LINKED 1A, SEVERE, WITH INFANTILE OR EARLY CHILDHOOD ONSET 		0.800 GeneticVariation UNIPROT
dbSNP: rs122458142
rs122458142
Entrez Id: 2273
Gene Symbol: FHL1
FHL1
CUI: C4225423
Disease:
REDUCING BODY MYOPATHY, X-LINKED 1A, SEVERE, WITH INFANTILE OR EARLY CHILDHOOD ONSET 		T 0.800 CausalMutation CLINVAR