rs775865079
- Likely benign
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
A
G
T
Chromosome
10
Location
78033913
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_033022.4(RPS24):c.3+9C>T
Allele
T
Clinical Significance
Likely benign