rs1584853041
- Likely benign
Your Genotype
Sign InDescription
Reference Allele
A
Alternative Allele
G
Chromosome
7
Location
87531300
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_001348946.2(ABCB1):c.2679T>C (p.Ser893=)
Allele
G
Clinical Significance
Likely benign