rs111943857
- Likely benign
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
T
Chromosome
13
Location
39660848
Variant Type
SNP
Genes
ClinVar
Name
NM_020751.3(COG6):c.336C>T (p.Ser112=)
Allele
T
Clinical Significance
Likely benign