rs138700050
- Likely benign
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
T
Chromosome
8
Location
69755469
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_030958.3(SLCO5A1):c.1213G>A (p.Ala405Thr)
Allele
T
Clinical Significance
Likely benign