rs1601879433
- Likely benign
Your Genotype
Sign InDescription
Reference Allele
A
Alternative Allele
T
Chromosome
22
Location
37974173
Variant Type
SNP
Phenotypes
ClinVar
Name
NM_006941.4(SOX10):c.723T>A (p.Pro241=)
Allele
T
Clinical Significance
Likely benign