rs1601879005
- Likely benign
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
C
Chromosome
22
Location
37973867
Variant Type
SNP
Phenotypes
ClinVar
Name
NM_006941.4(SOX10):c.1029C>G (p.Pro343=)
Allele
C
Clinical Significance
Likely benign