rs11538945
- Benign/Likely benign
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
T
Chromosome
19
Location
7639096
Variant Type
SNP
Genes
ClinVar
Name
NM_006949.4(STXBP2):c.165C>T (p.Ile55=)
Allele
T
Clinical Significance
Benign/Likely benign