rs1601886756
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
A
Chromosome
22
Location
37983456
Variant Type
SNP
Phenotypes
ClinVar
Name
NM_006941.4(SOX10):c.329C>T (p.Ala110Val)
Allele
A
Clinical Significance
Uncertain significance