rs199843908
- Likely benign
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
A
Chromosome
7
Location
87515438
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_001348946.2(ABCB1):c.3085-10C>T
Allele
A
Clinical Significance
Likely benign