rs377261686
- Likely benign
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
T
Chromosome
X
Location
154364888
Variant Type
SNP
Genes
ClinVar
Name
NM_001110556.2(FLNA):c.1761G>A (p.Glu587=)
Allele
T
Clinical Significance
Likely benign