rs1367848310
- Likely benign
Your Genotype
Sign InDescription
Synonymous alterations with insufficient evidence to classify as benign
Reference Allele
C
Alternative Allele
G
T
Chromosome
16
Location
2088538
Variant Type
SNP
ClinVar
Name
NM_000548.5(TSC2):c.5352C>T (p.Pro1784=)
Allele
T
Clinical Significance
Likely benign