rs899337295
- Likely benign
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
A
Chromosome
2
Location
5693933
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_003108.4(SOX11):c.1212G>A (p.Glu404=)
Allele
A
Clinical Significance
Likely benign