rs1240034111
- Likely benign
Your Genotype
Sign InDescription
Reference Allele
A
Alternative Allele
C
G
Chromosome
10
Location
78035687
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_033022.4(RPS24):c.246A>C (p.Ala82=)
Allele
C
Clinical Significance
Likely benign