rs34379884
- Likely benign
- not provided
Your Genotype
Sign InDescription
Reference Allele
T
Alternative Allele
C
G
Chromosome
16
Location
2088737
Variant Type
SNP
Phenotypes
ClinVar
Name
NM_000548.5(TSC2):c.*127T>C
Allele
C
Clinical Significance
Likely benign
Name
NM_000548.5(TSC2):c.*127T>G
Allele
G
Clinical Significance
not provided