rs139885563
- Likely benign
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
A
C
T
Chromosome
2
Location
5692784
Variant Type
SNP
Phenotypes
ClinVar
Name
NM_003108.4(SOX11):c.63G>T (p.Thr21=)
Allele
T
Clinical Significance
Likely benign