rs45517417
- not provided
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
T
Chromosome
16
Location
2088404
Variant Type
SNP
Phenotypes
ClinVar
Name
NM_000548.5(TSC2):c.5260-42C>T
Allele
T
Clinical Significance
not provided
C
T
16
2088404
SNP
NM_000548.5(TSC2):c.5260-42C>T
T
not provided