rs139181869
- Benign
Your Genotype
Sign InDescription
Reference Allele
A
Alternative Allele
G
Chromosome
10
Location
78037277
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_033022.4(RPS24):c.363A>G (p.Ala121=)
Allele
G
Clinical Significance
Benign
A
G
10
78037277
SNP
NM_033022.4(RPS24):c.363A>G (p.Ala121=)
G
Benign