rs773109683
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
T
Chromosome
22
Location
37974128
Variant Type
SNP
Phenotypes
ClinVar
Name
NM_006941.4(SOX10):c.768G>A (p.Pro256=)
Allele
T
Clinical Significance
Uncertain significance