rs2032582
- Benign
- Benign
Your Genotype
Sign InDescription
This variant is considered likely benign or benign based on one or more of the following criteria: it is a conservative change, it occurs at a poorly conserved position in the protein, it is predicted to be benign by multiple in silico algorithms, and/or has population frequency not consistent with disease.
Reference Allele
A
Alternative Allele
C
T
Chromosome
7
Location
87531302
Variant Type
SNP
Genes
ClinVar
Name
NM_001348946.2(ABCB1):c.2677T>G (p.Ser893Ala)
Allele
C
Clinical Significance
Benign
Name
NM_001348946.2(ABCB1):c.2677T>A (p.Ser893Thr)
Allele
T
Clinical Significance
Benign