rs1553327954
- Pathogenic
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
A
Chromosome
2
Location
5693512
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_003108.4(SOX11):c.791C>A (p.Ser264Ter)
Allele
A
Clinical Significance
Pathogenic