rs1555939426
- Likely pathogenic
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
C
Chromosome
22
Location
37983421
Variant Type
SNP
Phenotypes
ClinVar
Name
NM_006941.4(SOX10):c.364C>G (p.Leu122Val)
Allele
C
Clinical Significance
Likely pathogenic