rs866336771
- Uncertain significance
Your Genotype
Sign InDescription
This variant was determined to be of uncertain significance according to ACMG Guidelines, 2015 [PMID:25741868].
Reference Allele
A
Alternative Allele
T
Chromosome
13
Location
39660811
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_020751.3(COG6):c.299A>T (p.Glu100Val)
Allele
T
Clinical Significance
Uncertain significance