rs142227692
- Benign
Your Genotype
Sign InDescription
Reference Allele
T
Alternative Allele
C
Chromosome
8
Location
69761829
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_030958.3(SLCO5A1):c.954A>G (p.Leu318=)
Allele
C
Clinical Significance
Benign