rs782701643
- Benign/Likely benign
Your Genotype
Sign InDescription
In silico models in agreement (benign);Synonymous alterations with insufficient evidence to classify as benign
Reference Allele
G
Alternative Allele
A
Chromosome
X
Location
154367506
Variant Type
SNP
Genes
ClinVar
Name
NM_001110556.2(FLNA):c.759C>T (p.Asp253=)
Allele
A
Clinical Significance
Benign/Likely benign