rs1397030516
- Pathogenic
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
T
Chromosome
22
Location
38112503
Variant Type
SNP
Phenotypes
ClinVar
Name
NM_003560.4(PLA2G6):c.2276+1G>A
Allele
T
Clinical Significance
Pathogenic
C
T
22
38112503
SNP
NM_003560.4(PLA2G6):c.2276+1G>A
T
Pathogenic