rs886039070
- Likely benign
Your Genotype
Sign InDescription
This alteration is classified as likely benign based on a combination of the following: population frequency, intact protein function, lack of segregation with disease, co-occurrence, RNA analysis, in silico models, amino acid conservation, lack of disease association in case-control studies, and/or the mechanism of disease or impacted region is inconsistent with a known cause of pathogenicity.
Reference Allele
G
Alternative Allele
T
Chromosome
X
Location
154366595
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_001110556.2(FLNA):c.1032C>A (p.Val344=)
Allele
T
Clinical Significance
Likely benign