rs746501349
- Likely benign
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
A
C
T
Chromosome
2
Location
5693510
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_003108.4(SOX11):c.789G>A (p.Pro263=)
Allele
A
Clinical Significance
Likely benign