rs187531407
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
A
G
T
Chromosome
9
Location
113283207
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_001244926.2(PRPF4):c.556C>G (p.Pro186Ala)
Allele
G
Clinical Significance
Uncertain significance