rs1332625359
- Uncertain significance
Your Genotype
Sign InDescription
This variant was classified as: Uncertain significance. The following ACMG criteria were applied in classifying this variant: PM2,PP3.
Reference Allele
T
Alternative Allele
G
Chromosome
22
Location
37974178
Variant Type
SNP
Phenotypes
ClinVar
Name
NM_006941.4(SOX10):c.718A>C (p.Thr240Pro)
Allele
G
Clinical Significance
Uncertain significance