rs151033757
- Likely benign
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
A
C
T
Chromosome
9
Location
113283203
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_001244926.2(PRPF4):c.552G>A (p.Ser184=)
Allele
A
Clinical Significance
Likely benign