rs201805132
- Conflicting interpretations of pathogenicity
Your Genotype
Sign InDescription
Reference Allele
T
Alternative Allele
C
Chromosome
10
Location
78035630
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_033022.4(RPS24):c.189T>C (p.His63=)
Allele
C
Clinical Significance
Conflicting interpretations of pathogenicity