rs886057495
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
A
Alternative Allele
T
Chromosome
22
Location
37974150
Variant Type
SNP
Phenotypes
ClinVar
Name
NM_006941.4(SOX10):c.746T>A (p.Leu249Gln)
Allele
T
Clinical Significance
Uncertain significance