rs1932462410
- Likely pathogenic
Your Genotype
Sign InDescription
Reference Allele
A
Alternative Allele
G
Chromosome
22
Location
37983399
Variant Type
SNP
Phenotypes
ClinVar
Name
NM_006941.4(SOX10):c.386T>C (p.Leu129Pro)
Allele
G
Clinical Significance
Likely pathogenic