rs762120606
- Likely benign
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
A
Chromosome
16
Location
2088609
Variant Type
SNP
Phenotypes
ClinVar
Name
NM_000548.5(TSC2):c.5423G>A (p.Ter1808=)
Allele
A
Clinical Significance
Likely benign