rs1557179325
- Pathogenic
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
T
Chromosome
X
Location
154366562
Variant Type
SNP
Genes
ClinVar
Name
NM_001110556.2(FLNA):c.1065G>A (p.Lys355=)
Allele
T
Clinical Significance
Pathogenic