rs760114613
- Likely benign
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
A
Chromosome
7
Location
87550543
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_001348946.2(ABCB1):c.1149C>T (p.His383=)
Allele
A
Clinical Significance
Likely benign