rs761830881
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
A
Chromosome
20
Location
10297001
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_130811.4(SNAP25):c.358G>A (p.Val120Ile)
Allele
A
Clinical Significance
Uncertain significance