FLNA NM_001456.3 exon 8 p.Thr402Ala (c.1204A>G): This variant has not been reported in the literature and is not present in large control databases. Evolutionary conservation and computational predictive tools for this variant are unclear. In summary, data on this variant is insufficient for disease classification. Therefore, the clinical significance of this variant is uncertain.

NM_001110556.2(FLNA):c.1204A>G (p.Thr402Ala)

Melnick-Needles syndrome

Cardiac valvular dysplasia, X-linked

Oto-palato-digital syndrome, type I

Oto-palato-digital syndrome, type II

FG syndrome 2

Terminal osseous dysplasia-pigmentary defects syndrome

Heterotopia, periventricular, X-linked dominant

Intestinal pseudoobstruction, neuronal, chronic idiopathic, X-linked

Frontometaphyseal dysplasia 1

rs1569551838

Your Genotype

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Alternative Allele

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