rs146054602
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
A
Alternative Allele
C
G
Chromosome
13
Location
39677522
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_020751.3(COG6):c.483A>C (p.Gln161His)
Allele
C
Clinical Significance
Uncertain significance