rs1555938395
- Pathogenic/Likely pathogenic
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
A
Chromosome
22
Location
37978041
Variant Type
SNP
ClinVar
Name
NM_006941.4(SOX10):c.523C>T (p.Pro175Ser)
Allele
A
Clinical Significance
Pathogenic/Likely pathogenic