rs150778647
- Benign
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
A
Chromosome
8
Location
69672988
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_030958.3(SLCO5A1):c.2428C>T (p.Leu810=)
Allele
A
Clinical Significance
Benign