rs1553327863
- Likely pathogenic
Your Genotype
Sign InDescription
Reference Allele
A
Alternative Allele
T
Chromosome
2
Location
5693232
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_003108.4(SOX11):c.511A>T (p.Lys171Ter)
Allele
T
Clinical Significance
Likely pathogenic