rs536767446
- Likely benign
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
A
C
Chromosome
2
Location
5693345
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_003108.4(SOX11):c.624G>A (p.Ser208=)
Allele
A
Clinical Significance
Likely benign