rs782240483
- Uncertain significance
Your Genotype
Sign InDescription
In silico analysis, which includes protein predictors and evolutionary conservation, supports a deleterious effect; Has not been previously published as pathogenic or benign to our knowledge
This variant was classified as: Uncertain significance. The available evidence on this variant's pathogenicity is insufficient or conflicting. The following ACMG criteria were applied in classifying this variant: PP3.
Reference Allele
A
Alternative Allele
G
Chromosome
X
Location
154368003
Variant Type
SNP
Genes
ClinVar
Name
NM_001110556.2(FLNA):c.461T>C (p.Met154Thr)
Allele
G
Clinical Significance
Uncertain significance