rs1269084486
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
A
Chromosome
19
Location
7561267
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_001166114.2(PNPLA6):c.3973G>A (p.Asp1325Asn)
Allele
A
Clinical Significance
Uncertain significance