rs200234059
- Likely benign
Your Genotype
Sign InDescription
This variant is considered likely benign or benign based on one or more of the following criteria: it is a conservative change, it occurs at a poorly conserved position in the protein, it is predicted to be benign by multiple in silico algorithms, and/or has population frequency not consistent with disease.
Reference Allele
A
Alternative Allele
G
Chromosome
19
Location
7559058
Variant Type
SNP
Genes
ClinVar
Name
NM_001166114.2(PNPLA6):c.3606A>G (p.Leu1202=)
Allele
G
Clinical Significance
Likely benign