rs587777479
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
A
Alternative Allele
G
Chromosome
2
Location
5693068
Variant Type
SNP
ClinVar
Name
NM_003108.4(SOX11):c.347A>G (p.Tyr116Cys)
Allele
G
Clinical Significance
Uncertain significance