rs575066383
- Likely benign
Your Genotype
Sign InDescription
Reference Allele
A
Alternative Allele
T
Chromosome
7
Location
87550846
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_001348946.2(ABCB1):c.1000-8T>A
Allele
T
Clinical Significance
Likely benign