rs1832103162
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
A
Chromosome
9
Location
113276569
Variant Type
SNP
Phenotypes
ClinVar
Name
NM_001244926.2(PRPF4):c.49G>A (p.Asp17Asn)
Allele
A
Clinical Significance
Uncertain significance