rs2235012
- Benign
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
G
T
Chromosome
7
Location
87549411
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_001348946.2(ABCB1):c.1662G>C (p.Leu554=)
Allele
G
Clinical Significance
Benign