rs45517420
- not provided
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
A
C
Chromosome
16
Location
2088551
Variant Type
SNP
ClinVar
Name
NM_000548.5(TSC2):c.5365G>C (p.Glu1789Gln)
Allele
C
Clinical Significance
not provided
Name
NM_000548.5(TSC2):c.5365G>A (p.Glu1789Lys)
Allele
A
Clinical Significance
Uncertain significance