rs138500876
- Likely benign
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
T
Chromosome
22
Location
37977960
Variant Type
SNP
Phenotypes
ClinVar
Name
NM_006941.4(SOX10):c.604G>A (p.Ala202Thr)
Allele
T
Clinical Significance
Likely benign