rs1932464388
- Pathogenic
Your Genotype
Sign InDescription
Reference Allele
T
Alternative Allele
C
Chromosome
22
Location
37983459
Variant Type
SNP
Phenotypes
ClinVar
Name
NM_006941.4(SOX10):c.326A>G (p.Asn109Ser)
Allele
C
Clinical Significance
Pathogenic