rs369439585
- Likely benign
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
A
C
Chromosome
22
Location
37977991
Variant Type
SNP
Phenotypes
ClinVar
Name
NM_006941.4(SOX10):c.573C>T (p.Pro191=)
Allele
A
Clinical Significance
Likely benign