rs1236012815
- Likely pathogenic
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
A
Chromosome
19
Location
7557191
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_001166114.2(PNPLA6):c.3304G>A (p.Ala1102Thr)
Allele
A
Clinical Significance
Likely pathogenic