rs13332221
- Benign
Your Genotype
Sign InDescription
This variant is considered likely benign or benign based on one or more of the following criteria: it is a conservative change, it occurs at a poorly conserved position in the protein, it is predicted to be benign by multiple in silico algorithms, and/or has population frequency not consistent with disease.
Reference Allele
C
Alternative Allele
T
Chromosome
16
Location
2088397
Variant Type
SNP
ClinVar
Name
NM_000548.5(TSC2):c.5260-49C>T
Allele
T
Clinical Significance
Benign