rs141262841
- Likely benign
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
A
Chromosome
22
Location
37973903
Variant Type
SNP
Phenotypes
ClinVar
Name
NM_006941.4(SOX10):c.993C>T (p.Ser331=)
Allele
A
Clinical Significance
Likely benign