rs745664459
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
A
Chromosome
22
Location
38112166
Variant Type
SNP
Phenotypes
ClinVar
Name
NM_003560.4(PLA2G6):c.2416C>T (p.Pro806Ser)
Allele
A
Clinical Significance
Uncertain significance