rs1555939459
- Likely pathogenic
Your Genotype
Sign InDescription
Reference Allele
T
Alternative Allele
A
Chromosome
22
Location
37983484
Variant Type
SNP
Phenotypes
ClinVar
Name
NM_006941.4(SOX10):c.301A>T (p.Lys101Ter)
Allele
A
Clinical Significance
Likely pathogenic