rs151298910
- Benign/Likely benign
- 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
2088277
Variant Type
SNP
ClinVar
Name
NM_000548.5(TSC2):c.5211C>T (p.Pro1737=)
Allele
T
Clinical Significance
Benign/Likely benign
Name
NM_000548.5(TSC2):c.5211C>A (p.Pro1737=)
Allele
A
Clinical Significance
Benign/Likely benign