rs1932482770
- Likely pathogenic
Your Genotype
Sign InDescription
Reference Allele
T
Alternative Allele
C
Chromosome
22
Location
37983784
Variant Type
SNP
Phenotypes
ClinVar
Name
NM_006941.4(SOX10):c.1A>G (p.Met1Val)
Allele
C
Clinical Significance
Likely pathogenic