rs1557179291
- Likely benign
Your Genotype
Sign InDescription
Synonymous alterations with insufficient evidence to classify as benign
Reference Allele
A
Alternative Allele
G
Chromosome
X
Location
154366465
Variant Type
SNP
Genes
ClinVar
Name
NM_001110556.2(FLNA):c.1071T>C (p.Thr357=)
Allele
G
Clinical Significance
Likely benign