rs1000008449
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
G
T
Chromosome
19
Location
7560692
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_001166114.2(PNPLA6):c.3744C>G (p.Ser1248Arg)
Allele
G
Clinical Significance
Uncertain significance