rs1198155966
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
A
T
Chromosome
19
Location
7561535
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_001166114.2(PNPLA6):c.4071G>T (p.Glu1357Asp)
Allele
T
Clinical Significance
Uncertain significance