rs1555441528
- Benign/Likely benign
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
G
Chromosome
16
Location
2088559
Variant Type
SNP
Phenotypes
ClinVar
Name
NM_000548.5(TSC2):c.5373C>G (p.Gly1791=)
Allele
G
Clinical Significance
Benign/Likely benign