rs372287381
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
T
Alternative Allele
G
Chromosome
9
Location
113283383
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_001244926.2(PRPF4):c.561-6T>G
Allele
G
Clinical Significance
Uncertain significance