rs780878126
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
T
Chromosome
19
Location
7559132
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_001166114.2(PNPLA6):c.3680G>T (p.Gly1227Val)
Allele
T
Clinical Significance
Uncertain significance