rs750390370
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
T
Chromosome
2
Location
5693672
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_003108.4(SOX11):c.951C>T (p.Asn317=)
Allele
T
Clinical Significance
Uncertain significance