rs1832108619
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
A
Chromosome
9
Location
113276680
Variant Type
SNP
Phenotypes
ClinVar
Name
NM_001244926.2(PRPF4):c.160G>A (p.Gly54Arg)
Allele
A
Clinical Significance
Uncertain significance