rs1557179648
- 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
Reference Allele
C
Alternative Allele
G
Chromosome
X
Location
154367918
Variant Type
SNP
Genes
ClinVar
Name
NM_001110556.2(FLNA):c.546G>C (p.Gln182His)
Allele
G
Clinical Significance
Uncertain significance