rs45477298
- not provided
- Conflicting interpretations of pathogenicity
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
A
T
Chromosome
16
Location
2088462
Variant Type
SNP
ClinVar
Name
NM_000548.5(TSC2):c.5276C>A (p.Ala1759Asp)
Allele
A
Clinical Significance
not provided
Name
NM_000548.5(TSC2):c.5276C>T (p.Ala1759Val)
Allele
T
Clinical Significance
Conflicting interpretations of pathogenicity