rs1394402504
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
A
Chromosome
22
Location
38112247
Variant Type
SNP
Phenotypes
ClinVar
Name
NM_003560.4(PLA2G6):c.2335G>T (p.Val779Phe)
Allele
A
Clinical Significance
Uncertain significance