rs1483584740
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
A
G
Chromosome
22
Location
38112576
Variant Type
SNP
Phenotypes
ClinVar
Name
NM_003560.4(PLA2G6):c.2204G>C (p.Cys735Ser)
Allele
G
Clinical Significance
Uncertain significance