rs886056986
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
T
Chromosome
20
Location
9479478
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_001377142.1(PLCB4):c.*469G>T
Allele
T
Clinical Significance
Uncertain significance