rs1601887413
- 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
T
Alternative Allele
G
Chromosome
22
Location
37983874
Variant Type
SNP
Phenotypes
ClinVar
Name
NM_006941.4(SOX10):c.-84-6A>C
Allele
G
Clinical Significance
Likely benign