rs35318751
- Benign
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
A
Chromosome
8
Location
69831912
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_030958.3(SLCO5A1):c.762C>T (p.Asp254=)
Allele
A
Clinical Significance
Benign
G
A
8
69831912
SNP
NM_030958.3(SLCO5A1):c.762C>T (p.Asp254=)
A
Benign