rs1569167607
- Pathogenic
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
C
Chromosome
22
Location
37973727
Variant Type
SNP
Phenotypes
ClinVar
Name
NM_006941.4(SOX10):c.1169C>G (p.Ser390Ter)
Allele
C
Clinical Significance
Pathogenic