rs202003366
- Likely benign
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
A
T
Chromosome
20
Location
10297037
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_130811.4(SNAP25):c.394G>A (p.Gly132Ser)
Allele
A
Clinical Significance
Likely benign