rs201308360
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
A
Alternative Allele
G
Chromosome
13
Location
39659365
Variant Type
SNP
Genes
ClinVar
Name
NM_020751.3(COG6):c.155A>G (p.Glu52Gly)
Allele
G
Clinical Significance
Uncertain significance