rs1569239288
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
A
Alternative Allele
G
Chromosome
22
Location
38112532
Variant Type
SNP
Phenotypes
ClinVar
Name
NM_003560.4(PLA2G6):c.2248T>C (p.Cys750Arg)
Allele
G
Clinical Significance
Uncertain significance