rs1932280017
- Pathogenic
Your Genotype
Sign InDescription
Reference Allele
T
Alternative Allele
A
Chromosome
22
Location
37978116
Variant Type
SNP
Phenotypes
ClinVar
Name
NM_006941.4(SOX10):c.448A>T (p.Lys150Ter)
Allele
A
Clinical Significance
Pathogenic