rs80078382
- Benign
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
A
C
Chromosome
8
Location
69673088
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_030958.3(SLCO5A1):c.2328C>G (p.Pro776=)
Allele
C
Clinical Significance
Benign