rs982803529
- Likely benign
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
A
C
Chromosome
16
Location
2088601
Variant Type
SNP
ClinVar
Name
NM_000548.5(TSC2):c.5415G>A (p.Glu1805=)
Allele
A
Clinical Significance
Likely benign
Name
NM_000548.5(TSC2):c.5415G>C (p.Glu1805Asp)
Allele
C
Clinical Significance
Uncertain significance