rs775383590
- Uncertain significance
Your Genotype
Sign InDescription
In silico analysis supports that this missense variant does not alter protein structure/function; Has not been previously published as pathogenic or benign to our knowledge
Reference Allele
C
Alternative Allele
G
Chromosome
10
Location
78035523
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_033022.4(RPS24):c.82C>G (p.Leu28Val)
Allele
G
Clinical Significance
Uncertain significance