rs587784354
- Likely pathogenic
Your Genotype
Sign InDescription
Reference Allele
A
Alternative Allele
T
Chromosome
22
Location
38112186
Variant Type
SNP
Phenotypes
ClinVar
Name
NM_003560.4(PLA2G6):c.2396T>A (p.Leu799His)
Allele
T
Clinical Significance
Likely pathogenic