rs768125081
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
T
Alternative Allele
C
Chromosome
19
Location
7560687
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_001166114.2(PNPLA6):c.3739T>C (p.Trp1247Arg)
Allele
C
Clinical Significance
Uncertain significance