rs1176067979
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
A
Alternative Allele
G
Chromosome
19
Location
7558913
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_001166114.2(PNPLA6):c.3461A>G (p.Glu1154Gly)
Allele
G
Clinical Significance
Uncertain significance