rs1060500967
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
A
Alternative Allele
C
Chromosome
16
Location
2088457
Variant Type
SNP
Phenotypes
ClinVar
Name
NM_000548.5(TSC2):c.5271A>C (p.Glu1757Asp)
Allele
C
Clinical Significance
Uncertain significance