rs782315270
- Likely benign
Your Genotype
Sign InDescription
Synonymous alterations with insufficient evidence to classify as benign
Reference Allele
G
Alternative Allele
A
Chromosome
X
Location
154368071
Variant Type
SNP
Genes
ClinVar
Name
NM_001110556.2(FLNA):c.393C>T (p.Asp131=)
Allele
A
Clinical Significance
Likely benign