rs757747030
- Likely benign
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
A
T
Chromosome
20
Location
9473275
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_001377142.1(PLCB4):c.3409-4G>T
Allele
T
Clinical Significance
Likely benign