rs55852620
- Benign
Your Genotype
Sign InDescription
Reference Allele
T
Alternative Allele
G
Chromosome
7
Location
87509444
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_001348946.2(ABCB1):c.3320A>C (p.Gln1107Pro)
Allele
G
Clinical Significance
Benign