rs1569551861
- Pathogenic/Likely pathogenic
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
A
Chromosome
X
Location
154367685
Variant Type
SNP
Genes
ClinVar
Name
NM_001110556.2(FLNA):c.676C>T (p.Arg226Ter)
Allele
A
Clinical Significance
Pathogenic/Likely pathogenic