rs1395936283
- Likely benign
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
A
Chromosome
22
Location
37983452
Variant Type
SNP
Phenotypes
ClinVar
Name
NM_006941.4(SOX10):c.333C>T (p.Phe111=)
Allele
A
Clinical Significance
Likely benign