rs782682232
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
A
Chromosome
X
Location
154365478
Variant Type
SNP
Genes
ClinVar
Name
NM_001110556.2(FLNA):c.1438C>T (p.Pro480Ser)
Allele
A
Clinical Significance
Uncertain significance