rs1932130190
- Pathogenic
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
A
Chromosome
22
Location
37973701
Variant Type
SNP
Phenotypes
ClinVar
Name
NM_006941.4(SOX10):c.1195C>T (p.Gln399Ter)
Allele
A
Clinical Significance
Pathogenic