rs1555441410
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
G
Chromosome
16
Location
2088527
Variant Type
SNP
Phenotypes
ClinVar
Name
NM_000548.5(TSC2):c.5341C>G (p.Pro1781Ala)
Allele
G
Clinical Significance
Uncertain significance