rs1555937400
- Pathogenic
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
A
Chromosome
22
Location
37973806
Variant Type
SNP
Phenotypes
ClinVar
Name
NM_006941.4(SOX10):c.1090C>T (p.Gln364Ter)
Allele
A
Clinical Significance
Pathogenic