rs778705470
- Uncertain significance
- no interpretation for the single variant
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
G
T
Chromosome
22
Location
38112226
Variant Type
SNP
Phenotypes
ClinVar
Name
NM_003560.4(PLA2G6):c.2356G>C (p.Glu786Gln)
Allele
G
Clinical Significance
Uncertain significance
Name
NM_003560.4(PLA2G6):c.2356G>A (p.Glu786Lys)
Allele
T
Clinical Significance
no interpretation for the single variant