rs587784350
- Pathogenic
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
A
Chromosome
22
Location
38112547
Variant Type
SNP
ClinVar
Name
NM_003560.4(PLA2G6):c.2233C>T (p.Arg745Trp)
Allele
A
Clinical Significance
Pathogenic
G
A
22
38112547
SNP
NM_003560.4(PLA2G6):c.2233C>T (p.Arg745Trp)
A
Pathogenic