rs1569169289
- Pathogenic
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
A
T
Chromosome
22
Location
37978077
Variant Type
SNP
Phenotypes
ClinVar
Name
NM_006941.4(SOX10):c.487C>T (p.Gln163Ter)
Allele
A
Clinical Significance
Pathogenic