rs148684386
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
A
Alternative Allele
C
Chromosome
9
Location
113282727
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_001244926.2(PRPF4):c.474A>C (p.Lys158Asn)
Allele
C
Clinical Significance
Uncertain significance