rs753273617
- Uncertain significance
Your Genotype
Sign InDescription
In silico analysis, which includes protein predictors and evolutionary conservation, supports that this variant does not alter protein structure/function; Has not been previously published as pathogenic or benign to our knowledge
Reference Allele
C
Alternative Allele
T
Chromosome
19
Location
7556540
Variant Type
SNP
Genes
ClinVar
Name
NM_001166114.2(PNPLA6):c.3181C>T (p.His1061Tyr)
Allele
T
Clinical Significance
Uncertain significance