rs779463513
- Likely benign
Your Genotype
Sign InDescription
Reference Allele
T
Alternative Allele
C
Chromosome
7
Location
87520781
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_001348946.2(ABCB1):c.2781A>G (p.Pro927=)
Allele
C
Clinical Significance
Likely benign