rs1932463844
- Likely pathogenic
Your Genotype
Sign InDescription
Reference Allele
A
Alternative Allele
C
Chromosome
22
Location
37983450
Variant Type
SNP
Phenotypes
ClinVar
Name
NM_006941.4(SOX10):c.335T>G (p.Met112Arg)
Allele
C
Clinical Significance
Likely pathogenic