rs1202026658
- Uncertain significance
Your Genotype
Sign InDescription
In silico analysis supports that this missense variant has a deleterious effect on protein structure/function; Has not been previously published as pathogenic or benign to our knowledge
Reference Allele
C
Alternative Allele
T
Chromosome
19
Location
7557201
Variant Type
SNP
Genes
ClinVar
Name
NM_001166114.2(PNPLA6):c.3314C>T (p.Thr1105Met)
Allele
T
Clinical Significance
Uncertain significance