rs11547858
- Likely benign
Your Genotype
Sign InDescription
In silico models in agreement (benign);Synonymous alterations with insufficient evidence to classify as benign
Reference Allele
C
Alternative Allele
A
T
Chromosome
20
Location
10275497
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_130811.4(SNAP25):c.6C>T (p.Ala2=)
Allele
T
Clinical Significance
Likely benign