rs1373797370
- Likely pathogenic
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
G
T
Chromosome
22
Location
37978112
Variant Type
SNP
Phenotypes
ClinVar
Name
NM_006941.4(SOX10):c.452G>C (p.Arg151Pro)
Allele
G
Clinical Significance
Likely pathogenic