rs772238193
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
A
C
Chromosome
9
Location
113278977
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_001244926.2(PRPF4):c.238G>C (p.Glu80Gln)
Allele
C
Clinical Significance
Uncertain significance