rs368227790
- Likely benign
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
A
Chromosome
X
Location
154366369
Variant Type
SNP
Genes
ClinVar
Name
NM_001110556.2(FLNA):c.1167C>T (p.Pro389=)
Allele
A
Clinical Significance
Likely benign