rs1567132521
- 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
G
T
Chromosome
16
Location
2088319
Variant Type
SNP
Phenotypes
ClinVar
Name
NM_000548.5(TSC2):c.5253C>G (p.Arg1751=)
Allele
G
Clinical Significance
Likely benign