rs146246780
- Benign
Your Genotype
Sign InDescription
Reference Allele
T
Alternative Allele
C
Chromosome
9
Location
113279036
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_001244926.2(PRPF4):c.297T>C (p.Asn99=)
Allele
C
Clinical Significance
Benign