rs363050
- Benign
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
A
Chromosome
20
Location
10253609
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_130811.4(SNAP25):c.-63-21820G>A
Allele
A
Clinical Significance
Benign
G
A
20
10253609
SNP
NM_130811.4(SNAP25):c.-63-21820G>A
A
Benign