GFAP Chromosome 17

Glial fibrillary acidic protein
83 variants 83 Health Risk

Upload your DNA to see your personal genotypes for variants in GFAP.

What This Gene Does
This gene encodes one of the major intermediate filament proteins of mature astrocytes. It is used as a marker to distinguish astrocytes from other glial cells during development. Mutations in this gene cause Alexander disease, a rare disorder of astrocytes in the central nervous system. Alternative splicing results in multiple transcript variants encoding distinct isoforms. [provided by RefSeq, Oct 2008]
Gene Info
Gene Group
Intermediate filaments Type III
Locus Type
gene with protein product
Location
17q21.31
Ensembl
ENSG00000131095
Associated Conditions (10)
Alexander disease
Inborn genetic diseases
Hereditary spastic paraplegia
GFAP-related disorder
Scoliosis
Progressive ventriculomegaly
Spastic paraplegia
intellectual disability
nystagmus
and obesity
Key Variants
All Variants (83)
RSID Category Clinical Significance Conditions
RS1185404768 Health Risk Conflicting classifications of pathogenicity Alexander disease, Alexander disease
RS146725018 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Alexander disease, Inborn genetic diseases
RS147282497 Health Risk Conflicting classifications of pathogenicity Alexander disease, Alexander disease
RS148887665 Health Risk Conflicting classifications of pathogenicity Hereditary spastic paraplegia, Hereditary spastic paraplegia
RS149353780 Health Risk Conflicting classifications of pathogenicity
RS149883728 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS151327900 Health Risk Conflicting classifications of pathogenicity
RS1555574517 Health Risk Conflicting classifications of pathogenicity
RS1567778698 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS180974014 Health Risk Conflicting classifications of pathogenicity Alexander disease, Alexander disease
RS201382676 Health Risk Conflicting classifications of pathogenicity GFAP-related disorder, GFAP-related disorder
RS201959936 Health Risk Conflicting classifications of pathogenicity
RS201998644 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS2508933141 Health Risk Conflicting classifications of pathogenicity Alexander disease, Alexander disease
RS267607507 Health Risk Conflicting classifications of pathogenicity Alexander disease, Alexander disease
RS267607510 Health Risk Conflicting classifications of pathogenicity Alexander disease, Alexander disease
RS267607518 Health Risk Conflicting classifications of pathogenicity Alexander disease, Alexander disease, Alexander disease
RS267607526 Health Risk Conflicting classifications of pathogenicity Alexander disease, Alexander disease
RS375692636 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS552590923 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Alexander disease, Inborn genetic diseases
RS56679084 Health Risk Conflicting classifications of pathogenicity Alexander disease, Alexander disease
RS748860341 Health Risk Conflicting classifications of pathogenicity Alexander disease, Alexander disease, Alexander disease
RS760672791 Health Risk Conflicting classifications of pathogenicity Alexander disease, Inborn genetic diseases, GFAP-related disorder
RS775524073 Health Risk Conflicting classifications of pathogenicity Alexander disease, Alexander disease
RS1057518685 Health Risk Likely pathogenic Alexander disease, Alexander disease
RS1057518828 Health Risk Likely pathogenic Scoliosis, Scoliosis
RS1421576880 Health Risk Likely pathogenic GFAP-related disorder, GFAP-related disorder
RS1555573462 Health Risk Likely pathogenic
RS1567773470 Health Risk Likely pathogenic Alexander disease, Alexander disease
RS1597853099 Health Risk Likely pathogenic Alexander disease, Alexander disease
RS2051680751 Health Risk Likely pathogenic
RS2145632623 Health Risk Likely pathogenic Progressive ventriculomegaly, Progressive ventriculomegaly
RS2145637388 Health Risk Likely pathogenic Alexander disease, Alexander disease
RS2508923016 Health Risk Likely pathogenic
RS2508933747 Health Risk Likely pathogenic
RS2508940444 Health Risk Likely pathogenic
RS2508948888 Health Risk Likely pathogenic Alexander disease, Alexander disease
RS2508949801 Health Risk Likely pathogenic Alexander disease, Alexander disease
RS2508949861 Health Risk Likely pathogenic
RS267607515 Health Risk Likely pathogenic Alexander disease, Alexander disease
RS571151302 Health Risk Likely pathogenic Alexander disease, Alexander disease
RS759844035 Health Risk Likely pathogenic Alexander disease, Alexander disease
RS797044569 Health Risk Likely pathogenic Alexander disease, Alexander disease
RS797044570 Health Risk Likely pathogenic Alexander disease, Alexander disease
RS121909717 Health Risk Pathogenic Alexander disease, Inborn genetic diseases, Alexander disease
RS121909718 Health Risk Pathogenic Alexander disease, Alexander disease
RS121909719 Health Risk Pathogenic Alexander disease, Alexander disease
RS121909720 Health Risk Pathogenic Alexander disease, Alexander disease
RS149404477 Health Risk Pathogenic
RS1597864461 Health Risk Pathogenic Alexander disease, Alexander disease
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