rs34148850
- Likely benign
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
T
Chromosome
8
Location
69832346
Variant Type
SNP
Genes
LOC101929759
Phenotypes
ClinVar
Name
NM_030958.3(SLCO5A1):c.328G>A (p.Ala110Thr)
Allele
T
Clinical Significance
Likely benign