rs28364274
- Benign
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
T
Chromosome
7
Location
87504335
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_001348946.2(ABCB1):c.3751G>A (p.Val1251Ile)
Allele
T
Clinical Significance
Benign