rs1932142815
- Pathogenic
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
T
Chromosome
22
Location
37973955
Variant Type
SNP
Phenotypes
ClinVar
Name
NM_006941.4(SOX10):c.941C>A (p.Ser314Ter)
Allele
T
Clinical Significance
Pathogenic