rs1603362453
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
A
Alternative Allele
T
Chromosome
X
Location
154364853
Variant Type
SNP
Genes
ClinVar
Name
NM_001110556.2(FLNA):c.1796T>A (p.Val599Glu)
Allele
T
Clinical Significance
Uncertain significance