rs372113435
- Likely benign
Your Genotype
Sign InDescription
Lines of evidence used in support of classification: Synonymous alterations with insufficient evidence to classify as benign,In silico models in agreement (benign)
In silico models in agreement (benign);Synonymous alterations with insufficient evidence to classify as benign
Reference Allele
G
Alternative Allele
A
T
Chromosome
X
Location
154366139
Variant Type
SNP
Genes
ClinVar
Name
NM_001110556.2(FLNA):c.1314C>T (p.Gly438=)
Allele
A
Clinical Significance
Likely benign