rs878854905
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
C
T
Chromosome
19
Location
7560716
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_001166114.2(PNPLA6):c.3768G>T (p.Met1256Ile)
Allele
T
Clinical Significance
Uncertain significance