rs104894188
- Pathogenic
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
T
Chromosome
10
Location
78037230
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_033022.4(RPS24):c.316C>T (p.Gln106Ter)
Allele
T
Clinical Significance
Pathogenic