rs1296348337
- Pathogenic
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
A
T
Chromosome
22
Location
38112529
Variant Type
SNP
Phenotypes
ClinVar
Name
NM_003560.4(PLA2G6):c.2251G>T (p.Glu751Ter)
Allele
A
Clinical Significance
Pathogenic