rs886044869
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
A
Chromosome
X
Location
154366426
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_001110556.2(FLNA):c.1110C>T (p.Phe370=)
Allele
A
Clinical Significance
Uncertain significance