rs1932464492
- Pathogenic
Your Genotype
Sign InDescription
Reference Allele
A
Alternative Allele
G
Chromosome
22
Location
37983462
Variant Type
SNP
Phenotypes
ClinVar
Name
NM_006941.4(SOX10):c.323T>C (p.Met108Thr)
Allele
G
Clinical Significance
Pathogenic