rs977939314
- Likely benign
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
A
T
Chromosome
2
Location
5693879
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_003108.4(SOX11):c.1158G>A (p.Ala386=)
Allele
A
Clinical Significance
Likely benign