rs370528124
- Conflicting interpretations of pathogenicity
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
T
Chromosome
22
Location
38112311
Variant Type
SNP
ClinVar
Name
NM_003560.4(PLA2G6):c.2277-6G>A
Allele
T
Clinical Significance
Conflicting interpretations of pathogenicity