rs780941797
- Benign/Likely benign
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
T
Chromosome
20
Location
10299415
Variant Type
SNP
Genes
ClinVar
Name
NM_130811.4(SNAP25):c.552+3G>T
Allele
T
Clinical Significance
Benign/Likely benign