rs776999856
- Benign
- Likely benign
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
A
C
Chromosome
22
Location
37973814
Variant Type
SNP
Phenotypes
ClinVar
Name
NM_006941.4(SOX10):c.1082C>T (p.Ala361Val)
Allele
A
Clinical Significance
Benign
Name
NM_006941.4(SOX10):c.1082C>G (p.Ala361Gly)
Allele
C
Clinical Significance
Likely benign