rs45517413
- not provided
Your Genotype
Sign InDescription
Reference Allele
T
Alternative Allele
C
Chromosome
16
Location
2088297
Variant Type
SNP
Phenotypes
ClinVar
Name
NM_000548.5(TSC2):c.5231T>C (p.Leu1744Pro)
Allele
C
Clinical Significance
not provided