rs542027378
- Likely benign
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
A
Chromosome
7
Location
87475454
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_000443.4(ABCB4):c.12G>T (p.Glu4Asp)
Allele
A
Clinical Significance
Likely benign