rs752945858
- Benign/Likely benign
Your Genotype
Sign InDescription
Synonymous alterations with insufficient evidence to classify as benign
Reference Allele
C
Alternative Allele
A
T
Chromosome
16
Location
2088460
Variant Type
SNP
ClinVar
Name
NM_000548.5(TSC2):c.5274C>T (p.Ala1758=)
Allele
T
Clinical Significance
Benign/Likely benign