rs368304859
- Likely benign
Your Genotype
Sign InDescription
Synonymous alterations with insufficient evidence to classify as benign
Reference Allele
C
Alternative Allele
T
Chromosome
X
Location
154364855
Variant Type
SNP
Genes
ClinVar
Name
NM_001110556.2(FLNA):c.1794G>A (p.Val598=)
Allele
T
Clinical Significance
Likely benign