rs141141860
- Conflicting interpretations of pathogenicity
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
G
T
Chromosome
7
Location
87475412
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_000443.4(ABCB4):c.54G>A (p.Glu18=)
Allele
T
Clinical Significance
Conflicting interpretations of pathogenicity