rs200623674
- Likely benign
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
A
T
Chromosome
16
Location
2088406
Variant Type
SNP
Phenotypes
ClinVar
Name
NM_000548.5(TSC2):c.5260-40C>T
Allele
T
Clinical Significance
Likely benign
C
A
T
16
2088406
SNP
NM_000548.5(TSC2):c.5260-40C>T
T
Likely benign