rs121909117
- Pathogenic
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
A
Chromosome
22
Location
37978094
Variant Type
SNP
Phenotypes
ClinVar
Name
NM_006941.4(SOX10):c.470C>T (p.Ala157Val)
Allele
A
Clinical Significance
Pathogenic