rs1020277168
- Likely benign
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
A
C
Chromosome
10
Location
78037211
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_033022.4(RPS24):c.297G>A (p.Lys99=)
Allele
A
Clinical Significance
Likely benign