rs1932279377
- Pathogenic
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
A
Chromosome
22
Location
37978101
Variant Type
SNP
Phenotypes
ClinVar
Name
NM_006941.4(SOX10):c.463G>T (p.Glu155Ter)
Allele
A
Clinical Significance
Pathogenic