rs370820622
- Benign/Likely benign
Your Genotype
Sign InDescription
Synonymous alterations with insufficient evidence to classify as benign
Reference Allele
T
Alternative Allele
C
Chromosome
16
Location
2088517
Variant Type
SNP
ClinVar
Name
NM_000548.5(TSC2):c.5331T>C (p.Pro1777=)
Allele
C
Clinical Significance
Benign/Likely benign