rs104894189
- Pathogenic
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
G
T
Chromosome
10
Location
78035394
Variant Type
SNP
Genes
ClinVar
Name
NM_033022.4(RPS24):c.46C>T (p.Arg16Ter)
Allele
T
Clinical Significance
Pathogenic
C
G
T
10
78035394
SNP
NM_033022.4(RPS24):c.46C>T (p.Arg16Ter)
T
Pathogenic