rs764180850
- Likely benign
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
G
Chromosome
22
Location
37973819
Variant Type
SNP
Phenotypes
ClinVar
Name
NM_006941.4(SOX10):c.1077G>C (p.Glu359Asp)
Allele
G
Clinical Significance
Likely benign