rs761162904
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
A
T
Chromosome
16
Location
2088450
Variant Type
SNP
Phenotypes
ClinVar
Name
NM_000548.5(TSC2):c.5264G>T (p.Cys1755Phe)
Allele
T
Clinical Significance
Uncertain significance