rs1388073236
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
G
T
Chromosome
2
Location
5693606
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_003108.4(SOX11):c.885C>G (p.Asp295Glu)
Allele
G
Clinical Significance
Uncertain significance