rs748785049
- Likely benign
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
T
Chromosome
20
Location
9435564
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_001377142.1(PLCB4):c.2529C>T (p.Ile843=)
Allele
T
Clinical Significance
Likely benign