rs1553327809
- Uncertain significance
Your Genotype
Sign InDescription
Lines of evidence used in support of classification: UNCERTAIN: Alteration(s) of Uncertain Clinical Significance Detected
Reference Allele
C
Alternative Allele
G
Chromosome
2
Location
5692960
Variant Type
SNP
Phenotypes
ClinVar
Name
NM_003108.4(SOX11):c.239C>G (p.Ser80Cys)
Allele
G
Clinical Significance
Uncertain significance