rs1588009545
- Likely benign
Your Genotype
Sign InDescription
Reference Allele
T
Alternative Allele
C
Chromosome
9
Location
113279102
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_001244926.2(PRPF4):c.363T>C (p.Phe121=)
Allele
C
Clinical Significance
Likely benign