rs747752100
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
A
Chromosome
19
Location
7559140
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_001166114.2(PNPLA6):c.3688G>A (p.Asp1230Asn)
Allele
A
Clinical Significance
Uncertain significance