rs35616937
- Benign
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
A
C
Chromosome
8
Location
69832363
Variant Type
SNP
Genes
LOC101929759
Phenotypes
ClinVar
Name
NM_030958.3(SLCO5A1):c.311C>G (p.Thr104Ser)
Allele
C
Clinical Significance
Benign