rs747614356
- Likely benign
Your Genotype
Sign InDescription
Reference Allele
A
Alternative Allele
G
T
Chromosome
16
Location
2088529
Variant Type
SNP
Phenotypes
ClinVar
Name
NM_000548.5(TSC2):c.5343A>G (p.Pro1781=)
Allele
G
Clinical Significance
Likely benign