rs751093717
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
A
T
Chromosome
2
Location
5693180
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_003108.4(SOX11):c.459C>T (p.Gly153=)
Allele
T
Clinical Significance
Uncertain significance