rs753386551
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
A
Chromosome
19
Location
7560702
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_001166114.2(PNPLA6):c.3754G>A (p.Val1252Ile)
Allele
A
Clinical Significance
Uncertain significance