rs2091217625
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
T
Alternative Allele
C
Chromosome
16
Location
2088585
Variant Type
SNP
Phenotypes
ClinVar
Name
NM_000548.5(TSC2):c.5399T>C (p.Val1800Ala)
Allele
C
Clinical Significance
Uncertain significance