rs1932150045
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
G
Chromosome
22
Location
37974121
Variant Type
SNP
Phenotypes
ClinVar
Name
NM_006941.4(SOX10):c.775G>C (p.Asp259His)
Allele
G
Clinical Significance
Uncertain significance