rs1401212310
- Likely benign
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
A
T
Chromosome
2
Location
5693249
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_003108.4(SOX11):c.528G>T (p.Ala176=)
Allele
T
Clinical Significance
Likely benign