rs1016478271
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
C
T
Chromosome
13
Location
39655735
Variant Type
SNP
Genes
ClinVar
Name
NM_020751.3(COG6):c.9G>C (p.Glu3Asp)
Allele
C
Clinical Significance
Uncertain significance