rs759728603
- Likely benign
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
A
Chromosome
22
Location
38112583
Variant Type
SNP
Phenotypes
ClinVar
Name
NM_003560.4(PLA2G6):c.2203-6C>T
Allele
A
Clinical Significance
Likely benign
G
A
22
38112583
SNP
NM_003560.4(PLA2G6):c.2203-6C>T
A
Likely benign