rs1060500918
- Uncertain significance
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
A
T
Chromosome
16
Location
2088589
Variant Type
SNP
Phenotypes
ClinVar
Name
NM_000548.5(TSC2):c.5403G>T (p.Glu1801Asp)
Allele
T
Clinical Significance
Uncertain significance
Name
NM_000548.5(TSC2):c.5403G>A (p.Glu1801=)
Allele
A
Clinical Significance
Uncertain significance