rs74756846
- Likely benign
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
T
Chromosome
2
Location
5693895
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_003108.4(SOX11):c.1174C>T (p.Leu392=)
Allele
T
Clinical Significance
Likely benign