rs757292336
- Likely benign
- Likely benign
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
G
T
Chromosome
16
Location
2088514
Variant Type
SNP
Phenotypes
ClinVar
Name
NM_000548.5(TSC2):c.5328C>T (p.Ala1776=)
Allele
T
Clinical Significance
Likely benign
Name
NM_000548.5(TSC2):c.5328C>G (p.Ala1776=)
Allele
G
Clinical Significance
Likely benign