rs1567133600
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
A
Alternative Allele
G
Chromosome
16
Location
2088470
Variant Type
SNP
Phenotypes
ClinVar
Name
NM_000548.5(TSC2):c.5284A>G (p.Asn1762Asp)
Allele
G
Clinical Significance
Uncertain significance