rs9282563
- Benign
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
A
Chromosome
7
Location
87531329
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_001348946.2(ABCB1):c.2650C>T (p.Leu884=)
Allele
A
Clinical Significance
Benign