rs374821573
- Likely benign
Your Genotype
Sign InDescription
This variant is considered likely benign or benign based on one or more of the following criteria: it is a conservative change, it occurs at a poorly conserved position in the protein, it is predicted to be benign by multiple in silico algorithms, and/or has population frequency not consistent with disease.
Reference Allele
C
Alternative Allele
A
G
T
Chromosome
13
Location
39655684
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_020751.3(COG6):c.-43C>T
Allele
T
Clinical Significance
Likely benign