rs144909284
- Likely benign
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
C
Chromosome
8
Location
69832441
Variant Type
SNP
Genes
LOC101929759
Phenotypes
ClinVar
Name
NM_030958.3(SLCO5A1):c.233C>G (p.Pro78Arg)
Allele
C
Clinical Significance
Likely benign