rs2024087885
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
A
Alternative Allele
C
Chromosome
19
Location
7561232
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_001166114.2(PNPLA6):c.3938A>C (p.Glu1313Ala)
Allele
C
Clinical Significance
Uncertain significance