rs1602051017
- Likely pathogenic
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
T
Chromosome
22
Location
38112232
Variant Type
SNP
Phenotypes
ClinVar
Name
NM_003560.4(PLA2G6):c.2350G>A (p.Glu784Lys)
Allele
T
Clinical Significance
Likely pathogenic