rs1555441455
- Uncertain significance
- Uncertain significance
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
A
Alternative Allele
C
G
T
Chromosome
16
Location
2088539
Variant Type
SNP
Phenotypes
ClinVar
Name
NM_000548.5(TSC2):c.5353A>T (p.Thr1785Ser)
Allele
T
Clinical Significance
Uncertain significance
Name
NM_000548.5(TSC2):c.5353A>C (p.Thr1785Pro)
Allele
C
Clinical Significance
Uncertain significance
Name
NM_000548.5(TSC2):c.5353A>G (p.Thr1785Ala)
Allele
G
Clinical Significance
Uncertain significance