rs991368727
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
T
Chromosome
2
Location
5693830
Variant Type
SNP
Genes
ClinVar
Name
NM_003108.4(SOX11):c.1109C>T (p.Ser370Phe)
Allele
T
Clinical Significance
Uncertain significance