rs34295070
- Benign
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
G
T
Chromosome
8
Location
69755467
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_030958.3(SLCO5A1):c.1215G>A (p.Ala405=)
Allele
T
Clinical Significance
Benign