rs45517422
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
C
Chromosome
16
Location
2088562
Variant Type
SNP
ClinVar
Name
NM_000548.5(TSC2):c.5376G>C (p.Gln1792His)
Allele
C
Clinical Significance
Uncertain significance