rs1589326814
- Likely benign
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
T
Chromosome
10
Location
78035606
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_033022.4(RPS24):c.165C>T (p.Ile55=)
Allele
T
Clinical Significance
Likely benign