rs1304574596
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
T
Chromosome
2
Location
5692946
Variant Type
SNP
Phenotypes
ClinVar
Name
NM_003108.4(SOX11):c.225C>T (p.His75=)
Allele
T
Clinical Significance
Uncertain significance