rs761181064
- Conflicting interpretations of pathogenicity
Your Genotype
Sign InDescription
In silico analysis supports that this missense variant does not alter protein structure/function
Reference Allele
C
Alternative Allele
T
Chromosome
16
Location
2088494
Variant Type
SNP
ClinVar
Name
NM_000548.5(TSC2):c.5308C>T (p.Pro1770Ser)
Allele
T
Clinical Significance
Conflicting interpretations of pathogenicity