rs770105416
- Likely benign
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
T
Chromosome
22
Location
37973815
Variant Type
SNP
Phenotypes
ClinVar
Name
NM_006941.4(SOX10):c.1081G>A (p.Ala361Thr)
Allele
T
Clinical Significance
Likely benign