rs760539449
- Likely pathogenic
Your Genotype
Sign InDescription
Reference Allele
T
Alternative Allele
C
Chromosome
22
Location
37974064
Variant Type
SNP
Phenotypes
ClinVar
Name
NM_006941.4(SOX10):c.832A>G (p.Ile278Val)
Allele
C
Clinical Significance
Likely pathogenic